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: CA1879978237
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814154A= , CM000671.2:g.127814154A= GRCh38
NC_000009.11:g.130576433A= , CM000671.1:g.130576433A= GRCh37
NC_000009.10:g.129616254A= NCBI36
NG_009551.1:g.45615T= , LRG_589:g.45615T=
NG_023245.1:g.16280A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467826.5:n.710-54A=
XM_005251864.2:c.1484-54A= XP_005251921.1:n.1484-54A=
XM_005251864.4:c.1484-54A= XP_005251921.1:n.1484-54A=
XM_017014565.2:c.1334-54A= XP_016870054.1:n.1334-54A=
XR_242582.2:n.1381-54A=
XR_242582.4:n.1379-54A=