Canonical Allele Identifier: CA1504945081

Gene: FGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589439_154589440delinsAG , CM000666.2:g.154589439_154589440delinsAG	GRCh38
NC_000004.11:g.155510591_155510592delinsAG , CM000666.1:g.155510591_155510592delinsAG	GRCh37
NC_000004.10:g.155730041_155730042delinsAG	NCBI36
NG_008832.1:g.6306_6307delinsCT , LRG_557:g.6306_6307delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.177_178delinsCT	ENSP00000498441.1:p.Asp59=
ENST00000403106.8:c.177_178delinsCT MANE Select	ENSP00000385981.3:p.Asp59=
ENST00000651975.1:c.177_178delinsCT	ENSP00000498441.1:p.Asp59=
ENST00000302053.7:c.177_178delinsCT	ENSP00000306361.3:p.Asp59=
ENST00000403106.7:c.177_178delinsCT	ENSP00000385981.3:p.Asp59=
ENST00000622532.1:c.177_178delinsCT	ENSP00000478487.1:p.Asp59=
NM_000508.3:c.177_178delinsCT , LRG_557t1:c.177_178delinsCT	NP_000499.1:p.Asp59=
NM_021871.2:c.177_178delinsCT , LRG_557t2:c.177_178delinsCT	NP_068657.1:p.Asp59=
NM_000508.4:c.177_178delinsCT	NP_000499.1:p.Asp59=
NM_021871.3:c.177_178delinsCT	NP_068657.1:p.Asp59=
NM_021871.4:c.177_178delinsCT MANE Select	NP_068657.1:p.Asp59=
NM_000508.5:c.177_178delinsCT	NP_000499.1:p.Asp59=