Canonical Allele Identifier: CA1504945058

Gene: FGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589400_154589404delinsGGGAA , CM000666.2:g.154589400_154589404delinsGGGAA	GRCh38
NC_000004.11:g.155510552_155510556delinsGGGAA , CM000666.1:g.155510552_155510556delinsGGGAA	GRCh37
NC_000004.10:g.155730002_155730006delinsGGGAA	NCBI36
NG_008832.1:g.6342_6346delinsTTCCC , LRG_557:g.6342_6346delinsTTCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.180+33_180+37delinsTTCCC	ENSP00000498441.1:n.180+33_180+37delinsTTCCC
ENST00000403106.8:c.180+33_180+37delinsTTCCC MANE Select	ENSP00000385981.3:n.180+33_180+37delinsTTCCC
ENST00000651975.1:c.180+33_180+37delinsTTCCC	ENSP00000498441.1:n.180+33_180+37delinsTTCCC
ENST00000302053.7:c.180+33_180+37delinsTTCCC	ENSP00000306361.3:n.180+33_180+37delinsTTCCC
ENST00000403106.7:c.180+33_180+37delinsTTCCC	ENSP00000385981.3:n.180+33_180+37delinsTTCCC
ENST00000622532.1:c.180+33_180+37delinsTTCCC	ENSP00000478487.1:n.180+33_180+37delinsTTCCC
NM_000508.3:c.180+33_180+37delinsTTCCC , LRG_557t1:c.180+33_180+37delinsTTCCC	NP_000499.1:n.180+33_180+37delinsTTCCC
NM_021871.2:c.180+33_180+37delinsTTCCC , LRG_557t2:c.180+33_180+37delinsTTCCC	NP_068657.1:n.180+33_180+37delinsTTCCC
NM_000508.4:c.180+33_180+37delinsTTCCC	NP_000499.1:n.180+33_180+37delinsTTCCC
NM_021871.3:c.180+33_180+37delinsTTCCC	NP_068657.1:n.180+33_180+37delinsTTCCC
NM_021871.4:c.180+33_180+37delinsTTCCC MANE Select	NP_068657.1:n.180+33_180+37delinsTTCCC
NM_000508.5:c.180+33_180+37delinsTTCCC	NP_000499.1:n.180+33_180+37delinsTTCCC