Canonical Allele Identifier: CA108760656

Gene: FGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585361C>T , CM000666.2:g.154585361C>T	GRCh38
NC_000004.11:g.155506513C>T , CM000666.1:g.155506513C>T	GRCh37
NC_000004.10:g.155725963C>T	NCBI36
NG_008832.1:g.10385G>A , LRG_557:g.10385G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021871.4:c.*133G>A MANE Select	NP_068657.1:n.*133G>A
ENST00000403106.8:c.*133G>A MANE Select	ENSP00000385981.3:n.*133G>A
NM_000508.3:c.1891+177G>A , LRG_557t1:c.1891+177G>A	NP_000499.1:n.1891+177G>A
NM_000508.4:c.1891+177G>A	NP_000499.1:n.1891+177G>A
NM_000508.5:c.1891+177G>A	NP_000499.1:n.1891+177G>A
NM_021871.2:c.*133G>A , LRG_557t2:c.*133G>A	NP_068657.1:n.*133G>A
NM_021871.3:c.*133G>A	NP_068657.1:n.*133G>A
ENST00000302053.7:c.1891+177G>A	ENSP00000306361.3:n.1891+177G>A
ENST00000403106.7:c.*133G>A	ENSP00000385981.3:n.*133G>A
ENST00000622532.1:c.*123G>A	ENSP00000478487.1:n.*123G>A
ENST00000651975.1:c.1891+177G>A	ENSP00000498441.1:n.1891+177G>A
ENST00000651975.2:c.1891+177G>A	ENSP00000498441.1:n.1891+177G>A