Canonical Allele Identifier: CA126455

Gene: FGA

Linked Data

• ClinVar Variation Id: 16397
• ClinVar RCV Id: RCV000017823
• dbSNP Id: rs121909604
• MyVariant Identifiers: chr4:g.155510693C>T (hg19) ; chr4:g.154589541C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589541C>T , CM000666.2:g.154589541C>T	GRCh38
NC_000004.11:g.155510693C>T , CM000666.1:g.155510693C>T	GRCh37
NC_000004.10:g.155730143C>T	NCBI36
NG_008832.1:g.6205G>A , LRG_557:g.6205G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.76G>A	ENSP00000498441.1:p.Asp26Asn
ENST00000403106.8:c.76G>A MANE Select	ENSP00000385981.3:p.Asp26Asn
ENST00000651975.1:c.76G>A	ENSP00000498441.1:p.Asp26Asn
ENST00000302053.7:c.76G>A	ENSP00000306361.3:p.Asp26Asn
ENST00000403106.7:c.76G>A	ENSP00000385981.3:p.Asp26Asn
ENST00000622532.1:c.76G>A	ENSP00000478487.1:p.Asp26Asn
NM_000508.3:c.76G>A , LRG_557t1:c.76G>A	NP_000499.1:p.Asp26Asn
NM_021871.2:c.76G>A , LRG_557t2:c.76G>A	NP_068657.1:p.Asp26Asn
NM_000508.4:c.76G>A	NP_000499.1:p.Asp26Asn
NM_021871.3:c.76G>A	NP_068657.1:p.Asp26Asn
NM_021871.4:c.76G>A MANE Select	NP_068657.1:p.Asp26Asn
NM_000508.5:c.76G>A	NP_000499.1:p.Asp26Asn