Canonical Allele Identifier: CA441815623

Gene: FGA

Linked Data

• dbSNP Id: rs1730821920
• MyVariant Identifiers: chr4:g.155510709T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589557T>A , CM000666.2:g.154589557T>A	GRCh38
NC_000004.11:g.155510709T>A , CM000666.1:g.155510709T>A	GRCh37
NC_000004.10:g.155730159T>A	NCBI36
NG_008832.1:g.6189A>T , LRG_557:g.6189A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.60A>T	ENSP00000498441.1:p.Ala20=
ENST00000403106.8:c.60A>T MANE Select	ENSP00000385981.3:p.Ala20=
ENST00000651975.1:c.60A>T	ENSP00000498441.1:p.Ala20=
ENST00000302053.7:c.60A>T	ENSP00000306361.3:p.Ala20=
ENST00000403106.7:c.60A>T	ENSP00000385981.3:p.Ala20=
ENST00000622532.1:c.60A>T	ENSP00000478487.1:p.Ala20=
NM_000508.3:c.60A>T , LRG_557t1:c.60A>T	NP_000499.1:p.Ala20=
NM_021871.2:c.60A>T , LRG_557t2:c.60A>T	NP_068657.1:p.Ala20=
NM_000508.4:c.60A>T	NP_000499.1:p.Ala20=
NM_021871.3:c.60A>T	NP_068657.1:p.Ala20=
NM_021871.4:c.60A>T MANE Select	NP_068657.1:p.Ala20=
NM_000508.5:c.60A>T	NP_000499.1:p.Ala20=