Canonical Allele Identifier: CA1504944912
Gene: FGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154589102G= , CM000666.2:g.154589102G= GRCh38
NC_000004.11:g.155510254G= , CM000666.1:g.155510254G= GRCh37
NC_000004.10:g.155729704G= NCBI36
NG_008832.1:g.6644C= , LRG_557:g.6644C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651975.2:c.181-126C= ENSP00000498441.1:n.181-126C=
ENST00000403106.8:c.181-126C= MANE Select ENSP00000385981.3:n.181-126C=
ENST00000651975.1:c.181-126C= ENSP00000498441.1:n.181-126C=
ENST00000302053.7:c.181-126C= ENSP00000306361.3:n.181-126C=
ENST00000403106.7:c.181-126C= ENSP00000385981.3:n.181-126C=
ENST00000622532.1:c.181-126C= ENSP00000478487.1:n.181-126C=
NM_000508.3:c.181-126C= , LRG_557t1:c.181-126C= NP_000499.1:n.181-126C=
NM_021871.2:c.181-126C= , LRG_557t2:c.181-126C= NP_068657.1:n.181-126C=
NM_000508.4:c.181-126C= NP_000499.1:n.181-126C=
NM_021871.3:c.181-126C= NP_068657.1:n.181-126C=
NM_021871.4:c.181-126C= MANE Select NP_068657.1:n.181-126C=
NM_000508.5:c.181-126C= NP_000499.1:n.181-126C=