Canonical Allele Identifier: CA3115007

Gene: FGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585511G>C , CM000666.2:g.154585511G>C	GRCh38
NC_000004.11:g.155506663G>C , CM000666.1:g.155506663G>C	GRCh37
NC_000004.10:g.155726113G>C	NCBI36
NG_008832.1:g.10235C>G , LRG_557:g.10235C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021871.4:c.1918C>G MANE Select	NP_068657.1:p.Pro640Ala
ENST00000403106.8:c.1918C>G MANE Select	ENSP00000385981.3:p.Pro640Ala
NM_000508.3:c.1891+27C>G , LRG_557t1:c.1891+27C>G	NP_000499.1:n.1891+27C>G
NM_000508.4:c.1891+27C>G	NP_000499.1:n.1891+27C>G
NM_000508.5:c.1891+27C>G	NP_000499.1:n.1891+27C>G
NM_021871.2:c.1918C>G , LRG_557t2:c.1918C>G	NP_068657.1:p.Pro640Ala
NM_021871.3:c.1918C>G	NP_068657.1:p.Pro640Ala
ENST00000302053.7:c.1891+27C>G	ENSP00000306361.3:n.1891+27C>G
ENST00000403106.7:c.1918C>G	ENSP00000385981.3:p.Pro640Ala
ENST00000622532.1:c.843C>G	ENSP00000478487.1:p.Ser281Arg
ENST00000651975.1:c.1891+27C>G	ENSP00000498441.1:n.1891+27C>G
ENST00000651975.2:c.1891+27C>G	ENSP00000498441.1:n.1891+27C>G