Canonical Allele Identifier: CA358533925
Gene: FGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154589525C>T , CM000666.2:g.154589525C>T GRCh38
NC_000004.11:g.155510677C>T , CM000666.1:g.155510677C>T GRCh37
NC_000004.10:g.155730127C>T NCBI36
NG_008832.1:g.6221G>A , LRG_557:g.6221G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651975.2:c.92G>A ENSP00000498441.1:p.Gly31Glu
ENST00000403106.8:c.92G>A MANE Select ENSP00000385981.3:p.Gly31Glu
ENST00000651975.1:c.92G>A ENSP00000498441.1:p.Gly31Glu
ENST00000302053.7:c.92G>A ENSP00000306361.3:p.Gly31Glu
ENST00000403106.7:c.92G>A ENSP00000385981.3:p.Gly31Glu
ENST00000622532.1:c.92G>A ENSP00000478487.1:p.Gly31Glu
NM_000508.3:c.92G>A , LRG_557t1:c.92G>A NP_000499.1:p.Gly31Glu
NM_021871.2:c.92G>A , LRG_557t2:c.92G>A NP_068657.1:p.Gly31Glu
NM_000508.4:c.92G>A NP_000499.1:p.Gly31Glu
NM_021871.3:c.92G>A NP_068657.1:p.Gly31Glu
NM_021871.4:c.92G>A MANE Select NP_068657.1:p.Gly31Glu
NM_000508.5:c.92G>A NP_000499.1:p.Gly31Glu