Canonical Allele Identifier: CA358529049

Gene: FGA

Linked Data

• gnomAD v4: 4-154585993-G-T
• MyVariant Identifiers: chr4:g.155507145G>T (hg19) ; chr4:g.154585993G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585993G>T , CM000666.2:g.154585993G>T	GRCh38
NC_000004.11:g.155507145G>T , CM000666.1:g.155507145G>T	GRCh37
NC_000004.10:g.155726595G>T	NCBI36
NG_008832.1:g.9753C>A , LRG_557:g.9753C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.1436C>A	ENSP00000498441.1:p.Thr479Asn
ENST00000403106.8:c.1436C>A MANE Select	ENSP00000385981.3:p.Thr479Asn
ENST00000651975.1:c.1436C>A	ENSP00000498441.1:p.Thr479Asn
ENST00000302053.7:c.1436C>A	ENSP00000306361.3:p.Thr479Asn
ENST00000403106.7:c.1436C>A	ENSP00000385981.3:p.Thr479Asn
ENST00000622532.1:c.644-283C>A	ENSP00000478487.1:n.644-283C>A
NM_000508.3:c.1436C>A , LRG_557t1:c.1436C>A	NP_000499.1:p.Thr479Asn
NM_021871.2:c.1436C>A , LRG_557t2:c.1436C>A	NP_068657.1:p.Thr479Asn
NM_000508.4:c.1436C>A	NP_000499.1:p.Thr479Asn
NM_021871.3:c.1436C>A	NP_068657.1:p.Thr479Asn
NM_021871.4:c.1436C>A MANE Select	NP_068657.1:p.Thr479Asn
NM_000508.5:c.1436C>A	NP_000499.1:p.Thr479Asn