Canonical Allele Identifier: CA358526772

Gene: FGA

Linked Data

• MyVariant Identifiers: chr4:g.155506860C>G (hg19) ; chr4:g.154585708C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585708C>G , CM000666.2:g.154585708C>G	GRCh38
NC_000004.11:g.155506860C>G , CM000666.1:g.155506860C>G	GRCh37
NC_000004.10:g.155726310C>G	NCBI36
NG_008832.1:g.10038G>C , LRG_557:g.10038G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.1721G>C	ENSP00000498441.1:p.Gly574Ala
ENST00000403106.8:c.1721G>C MANE Select	ENSP00000385981.3:p.Gly574Ala
ENST00000651975.1:c.1721G>C	ENSP00000498441.1:p.Gly574Ala
ENST00000302053.7:c.1721G>C	ENSP00000306361.3:p.Gly574Ala
ENST00000403106.7:c.1721G>C	ENSP00000385981.3:p.Gly574Ala
ENST00000622532.1:c.646G>C	ENSP00000478487.1:p.Val216Leu
NM_000508.3:c.1721G>C , LRG_557t1:c.1721G>C	NP_000499.1:p.Gly574Ala
NM_021871.2:c.1721G>C , LRG_557t2:c.1721G>C	NP_068657.1:p.Gly574Ala
NM_000508.4:c.1721G>C	NP_000499.1:p.Gly574Ala
NM_021871.3:c.1721G>C	NP_068657.1:p.Gly574Ala
NM_021871.4:c.1721G>C MANE Select	NP_068657.1:p.Gly574Ala
NM_000508.5:c.1721G>C	NP_000499.1:p.Gly574Ala