This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA590600968
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814156_127814157insCA , CM000671.2:g.127814156_127814157insCA GRCh38
NC_000009.11:g.130576435_130576436insCA , CM000671.1:g.130576435_130576436insCA GRCh37
NC_000009.10:g.129616256_129616257insCA NCBI36
NG_009551.1:g.45612_45613insTG , LRG_589:g.45612_45613insTG
NG_023245.1:g.16282_16283insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000467826.5:n.710-52_710-51insCA
XM_005251864.2:c.1484-52_1484-51insCA XP_005251921.1:n.1484-52_1484-51insCA
XM_005251864.4:c.1484-52_1484-51insCA XP_005251921.1:n.1484-52_1484-51insCA
XM_017014565.2:c.1334-52_1334-51insCA XP_016870054.1:n.1334-52_1334-51insCA
XR_242582.2:n.1381-52_1381-51insCA
XR_242582.4:n.1379-52_1379-51insCA