Canonical Allele Identifier: CA358526738

Gene: FGA

Linked Data

• COSMIC: COSM4122949 ; COSM4122950
• MyVariant Identifiers: chr4:g.155506853A>C (hg19) ; chr4:g.154585701A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585701A>C , CM000666.2:g.154585701A>C	GRCh38
NC_000004.11:g.155506853A>C , CM000666.1:g.155506853A>C	GRCh37
NC_000004.10:g.155726303A>C	NCBI36
NG_008832.1:g.10045T>G , LRG_557:g.10045T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.1728T>G	ENSP00000498441.1:p.Ser576=
ENST00000403106.8:c.1728T>G MANE Select	ENSP00000385981.3:p.Ser576=
ENST00000651975.1:c.1728T>G	ENSP00000498441.1:p.Ser576=
ENST00000302053.7:c.1728T>G	ENSP00000306361.3:p.Ser576=
ENST00000403106.7:c.1728T>G	ENSP00000385981.3:p.Ser576=
ENST00000622532.1:c.653T>G	ENSP00000478487.1:p.Leu218Arg
NM_000508.3:c.1728T>G , LRG_557t1:c.1728T>G	NP_000499.1:p.Ser576=
NM_021871.2:c.1728T>G , LRG_557t2:c.1728T>G	NP_068657.1:p.Ser576=
NM_000508.4:c.1728T>G	NP_000499.1:p.Ser576=
NM_021871.3:c.1728T>G	NP_068657.1:p.Ser576=
NM_021871.4:c.1728T>G MANE Select	NP_068657.1:p.Ser576=
NM_000508.5:c.1728T>G	NP_000499.1:p.Ser576=