Canonical Allele Identifier: CA126493
Community Standard Title: NM_021871.4(FGA):c.1622del (p.Val541AlafsTer27)
Gene: FGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154585807del , CM000666.2:g.154585807del GRCh38
NC_000004.11:g.155506959del , CM000666.1:g.155506959del GRCh37
NC_000004.10:g.155726409del NCBI36
NG_008832.1:g.9939del , LRG_557:g.9939del

Transcript Alleles

HGVS Amino-acid Change
NM_021871.4:c.1622del MANE Select NP_068657.1:p.Val541AlafsTer27
ENST00000403106.8:c.1622del MANE Select ENSP00000385981.3:p.Val541AlafsTer27
NM_000508.3:c.1622del , LRG_557t1:c.1622del NP_000499.1:p.Val541AlafsTer27
NM_000508.4:c.1622del NP_000499.1:p.Val541AlafsTer27
NM_000508.5:c.1622del NP_000499.1:p.Val541AlafsTer27
NM_021871.2:c.1622del , LRG_557t2:c.1622del NP_068657.1:p.Val541AlafsTer27
NM_021871.3:c.1622del NP_068657.1:p.Val541AlafsTer27
ENST00000302053.7:c.1622del ENSP00000306361.3:p.Val541AlafsTer27
ENST00000403106.7:c.1622del ENSP00000385981.3:p.Val541AlafsTer27
ENST00000622532.1:c.644-97del ENSP00000478487.1:n.644-97del
ENST00000651975.1:c.1622del ENSP00000498441.1:p.Val541AlafsTer27
ENST00000651975.2:c.1622del ENSP00000498441.1:p.Val541AlafsTer27