Canonical Allele Identifier: CA1504945111

Gene: FGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589501A= , CM000666.2:g.154589501A=	GRCh38
NC_000004.11:g.155510653A= , CM000666.1:g.155510653A=	GRCh37
NC_000004.10:g.155730103A=	NCBI36
NG_008832.1:g.6245T= , LRG_557:g.6245T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.116T=	ENSP00000498441.1:p.Val39=
ENST00000403106.8:c.116T= MANE Select	ENSP00000385981.3:p.Val39=
ENST00000651975.1:c.116T=	ENSP00000498441.1:p.Val39=
ENST00000302053.7:c.116T=	ENSP00000306361.3:p.Val39=
ENST00000403106.7:c.116T=	ENSP00000385981.3:p.Val39=
ENST00000622532.1:c.116T=	ENSP00000478487.1:p.Val39=
NM_000508.3:c.116T= , LRG_557t1:c.116T=	NP_000499.1:p.Val39=
NM_021871.2:c.116T= , LRG_557t2:c.116T=	NP_068657.1:p.Val39=
NM_000508.4:c.116T=	NP_000499.1:p.Val39=
NM_021871.3:c.116T=	NP_068657.1:p.Val39=
NM_021871.4:c.116T= MANE Select	NP_068657.1:p.Val39=
NM_000508.5:c.116T=	NP_000499.1:p.Val39=