Canonical Allele Identifier: CA789371618

Gene: FGA

Linked Data

• dbSNP Id: rs1360152351
• gnomAD v3: 4-154589277-ACAGTGCT-A
• gnomAD v4: 4-154589277-ACAGTGCT-A
• MyVariant Identifiers: chr4:g.155510430_155510436del (hg19) ; chr4:g.154589278_154589284del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589279_154589285del , CM000666.2:g.154589279_154589285del	GRCh38
NC_000004.11:g.155510431_155510437del , CM000666.1:g.155510431_155510437del	GRCh37
NC_000004.10:g.155729881_155729887del	NCBI36
NG_008832.1:g.6462_6468del , LRG_557:g.6462_6468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.180+153_180+159del	ENSP00000498441.1:n.180+153_180+159del
ENST00000403106.8:c.180+153_180+159del MANE Select	ENSP00000385981.3:n.180+153_180+159del
ENST00000651975.1:c.180+153_180+159del	ENSP00000498441.1:n.180+153_180+159del
ENST00000302053.7:c.180+153_180+159del	ENSP00000306361.3:n.180+153_180+159del
ENST00000403106.7:c.180+153_180+159del	ENSP00000385981.3:n.180+153_180+159del
ENST00000622532.1:c.180+153_180+159del	ENSP00000478487.1:n.180+153_180+159del
NM_000508.3:c.180+153_180+159del , LRG_557t1:c.180+153_180+159del	NP_000499.1:n.180+153_180+159del
NM_021871.2:c.180+153_180+159del , LRG_557t2:c.180+153_180+159del	NP_068657.1:n.180+153_180+159del
NM_000508.4:c.180+153_180+159del	NP_000499.1:n.180+153_180+159del
NM_021871.3:c.180+153_180+159del	NP_068657.1:n.180+153_180+159del
NM_021871.4:c.180+153_180+159del MANE Select	NP_068657.1:n.180+153_180+159del
NM_000508.5:c.180+153_180+159del	NP_000499.1:n.180+153_180+159del