Canonical Allele Identifier: CA2695204020

Gene: FGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585708_154585709delinsAA , CM000666.2:g.154585708_154585709delinsAA	GRCh38
NC_000004.11:g.155506860_155506861delinsAA , CM000666.1:g.155506860_155506861delinsAA	GRCh37
NC_000004.10:g.155726310_155726311delinsAA	NCBI36
NG_008832.1:g.10037_10038delinsTT , LRG_557:g.10037_10038delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.1720_1721delinsTT	ENSP00000498441.1:p.Gly574Phe
ENST00000403106.8:c.1720_1721delinsTT MANE Select	ENSP00000385981.3:p.Gly574Phe
ENST00000651975.1:c.1720_1721delinsTT	ENSP00000498441.1:p.Gly574Phe
ENST00000302053.7:c.1720_1721delinsTT	ENSP00000306361.3:p.Gly574Phe
ENST00000403106.7:c.1720_1721delinsTT	ENSP00000385981.3:p.Gly574Phe
ENST00000622532.1:c.645_646delinsTT	ENSP00000478487.1:p.Leu215_Val216delinsPheLeu
NM_000508.3:c.1720_1721delinsTT , LRG_557t1:c.1720_1721delinsTT	NP_000499.1:p.Gly574Phe
NM_021871.2:c.1720_1721delinsTT , LRG_557t2:c.1720_1721delinsTT	NP_068657.1:p.Gly574Phe
NM_000508.4:c.1720_1721delinsTT	NP_000499.1:p.Gly574Phe
NM_021871.3:c.1720_1721delinsTT	NP_068657.1:p.Gly574Phe
NM_021871.4:c.1720_1721delinsTT MANE Select	NP_068657.1:p.Gly574Phe
NM_000508.5:c.1720_1721delinsTT	NP_000499.1:p.Gly574Phe