Canonical Allele Identifier: CA2580616796

Gene: FGA

Linked Data

• ClinVar Variation Id: 16400
• ClinVar RCV Id: RCV000017841

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589513_154589514delinsTT , CM000666.2:g.154589513_154589514delinsTT	GRCh38
NC_000004.11:g.155510665_155510666delinsTT , CM000666.1:g.155510665_155510666delinsTT	GRCh37
NC_000004.10:g.155730115_155730116delinsTT	NCBI36
NG_008832.1:g.6232_6233delinsAA , LRG_557:g.6232_6233delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.103_104delinsAA	ENSP00000498441.1:p.Arg35Asn
ENST00000403106.8:c.103_104delinsAA MANE Select	ENSP00000385981.3:p.Arg35Asn
ENST00000651975.1:c.103_104delinsAA	ENSP00000498441.1:p.Arg35Asn
ENST00000302053.7:c.103_104delinsAA	ENSP00000306361.3:p.Arg35Asn
ENST00000403106.7:c.103_104delinsAA	ENSP00000385981.3:p.Arg35Asn
ENST00000622532.1:c.103_104delinsAA	ENSP00000478487.1:p.Arg35Asn
NM_000508.3:c.103_104delinsAA , LRG_557t1:c.103_104delinsAA	NP_000499.1:p.Arg35Asn
NM_021871.2:c.103_104delinsAA , LRG_557t2:c.103_104delinsAA	NP_068657.1:p.Arg35Asn
NM_000508.4:c.103_104delinsAA	NP_000499.1:p.Arg35Asn
NM_021871.3:c.103_104delinsAA	NP_068657.1:p.Arg35Asn
NM_021871.4:c.103_104delinsAA MANE Select	NP_068657.1:p.Arg35Asn
NM_000508.5:c.103_104delinsAA	NP_000499.1:p.Arg35Asn