Canonical Allele Identifier: CA358530579

Gene: FGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154586390G>C , CM000666.2:g.154586390G>C	GRCh38
NC_000004.11:g.155507542G>C , CM000666.1:g.155507542G>C	GRCh37
NC_000004.10:g.155726992G>C	NCBI36
NG_008832.1:g.9356C>G , LRG_557:g.9356C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021871.4:c.1039C>G MANE Select	NP_068657.1:p.Gln347Glu
ENST00000403106.8:c.1039C>G MANE Select	ENSP00000385981.3:p.Gln347Glu
NM_000508.3:c.1039C>G , LRG_557t1:c.1039C>G	NP_000499.1:p.Gln347Glu
NM_000508.4:c.1039C>G	NP_000499.1:p.Gln347Glu
NM_000508.5:c.1039C>G	NP_000499.1:p.Gln347Glu
NM_021871.2:c.1039C>G , LRG_557t2:c.1039C>G	NP_068657.1:p.Gln347Glu
NM_021871.3:c.1039C>G	NP_068657.1:p.Gln347Glu
ENST00000302053.7:c.1039C>G	ENSP00000306361.3:p.Gln347Glu
ENST00000403106.7:c.1039C>G	ENSP00000385981.3:p.Gln347Glu
ENST00000622532.1:c.643+396C>G	ENSP00000478487.1:n.643+396C>G
ENST00000651975.1:c.1039C>G	ENSP00000498441.1:p.Gln347Glu
ENST00000651975.2:c.1039C>G	ENSP00000498441.1:p.Gln347Glu