Canonical Allele Identifier: CA789371535

Gene: FGA

Linked Data

• dbSNP Id: rs1481581339
• gnomAD v3: 4-154589070-CTATCTCTTCCAG-C
• gnomAD v4: 4-154589070-CTATCTCTTCCAG-C
• MyVariant Identifiers: chr4:g.155510223_155510234del (hg19) ; chr4:g.154589071_154589082del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589071_154589082del , CM000666.2:g.154589071_154589082del	GRCh38
NC_000004.11:g.155510223_155510234del , CM000666.1:g.155510223_155510234del	GRCh37
NC_000004.10:g.155729673_155729684del	NCBI36
NG_008832.1:g.6664_6675del , LRG_557:g.6664_6675del

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.181-106_181-95del	ENSP00000498441.1:n.181-106_181-95del
ENST00000403106.8:c.181-106_181-95del MANE Select	ENSP00000385981.3:n.181-106_181-95del
ENST00000651975.1:c.181-106_181-95del	ENSP00000498441.1:n.181-106_181-95del
ENST00000302053.7:c.181-106_181-95del	ENSP00000306361.3:n.181-106_181-95del
ENST00000403106.7:c.181-106_181-95del	ENSP00000385981.3:n.181-106_181-95del
ENST00000622532.1:c.181-106_181-95del	ENSP00000478487.1:n.181-106_181-95del
NM_000508.3:c.181-106_181-95del , LRG_557t1:c.181-106_181-95del	NP_000499.1:n.181-106_181-95del
NM_021871.2:c.181-106_181-95del , LRG_557t2:c.181-106_181-95del	NP_068657.1:n.181-106_181-95del
NM_000508.4:c.181-106_181-95del	NP_000499.1:n.181-106_181-95del
NM_021871.3:c.181-106_181-95del	NP_068657.1:n.181-106_181-95del
NM_021871.4:c.181-106_181-95del MANE Select	NP_068657.1:n.181-106_181-95del
NM_000508.5:c.181-106_181-95del	NP_000499.1:n.181-106_181-95del