Canonical Allele Identifier: CA2672446702

Gene: FGA

Linked Data

• gnomAD v4: 4-154589401-GGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589403_154589405del , CM000666.2:g.154589403_154589405del	GRCh38
NC_000004.11:g.155510555_155510557del , CM000666.1:g.155510555_155510557del	GRCh37
NC_000004.10:g.155730005_155730007del	NCBI36
NG_008832.1:g.6342_6344del , LRG_557:g.6342_6344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.180+33_180+35del	ENSP00000498441.1:n.180+33_180+35del
ENST00000403106.8:c.180+33_180+35del MANE Select	ENSP00000385981.3:n.180+33_180+35del
ENST00000651975.1:c.180+33_180+35del	ENSP00000498441.1:n.180+33_180+35del
ENST00000302053.7:c.180+33_180+35del	ENSP00000306361.3:n.180+33_180+35del
ENST00000403106.7:c.180+33_180+35del	ENSP00000385981.3:n.180+33_180+35del
ENST00000622532.1:c.180+33_180+35del	ENSP00000478487.1:n.180+33_180+35del
NM_000508.3:c.180+33_180+35del , LRG_557t1:c.180+33_180+35del	NP_000499.1:n.180+33_180+35del
NM_021871.2:c.180+33_180+35del , LRG_557t2:c.180+33_180+35del	NP_068657.1:n.180+33_180+35del
NM_000508.4:c.180+33_180+35del	NP_000499.1:n.180+33_180+35del
NM_021871.3:c.180+33_180+35del	NP_068657.1:n.180+33_180+35del
NM_021871.4:c.180+33_180+35del MANE Select	NP_068657.1:n.180+33_180+35del
NM_000508.5:c.180+33_180+35del	NP_000499.1:n.180+33_180+35del