Canonical Allele Identifier: CA555606754

Gene: FGA

Linked Data

• dbSNP Id: rs1560827789
• gnomAD v2: 4-155510552-GGGAA-G
• gnomAD v4: 4-154589400-GGGAA-G
• MyVariant Identifiers: chr4:g.155510553_155510556del (hg19) ; chr4:g.154589401_154589404del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589405_154589408del , CM000666.2:g.154589405_154589408del	GRCh38
NC_000004.11:g.155510557_155510560del , CM000666.1:g.155510557_155510560del	GRCh37
NC_000004.10:g.155730007_155730010del	NCBI36
NG_008832.1:g.6342_6345del , LRG_557:g.6342_6345del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651975.2:c.180+33_180+36del	ENSP00000498441.1:n.180+33_180+36del
ENST00000403106.8:c.180+33_180+36del MANE Select	ENSP00000385981.3:n.180+33_180+36del
ENST00000651975.1:c.180+33_180+36del	ENSP00000498441.1:n.180+33_180+36del
ENST00000302053.7:c.180+33_180+36del	ENSP00000306361.3:n.180+33_180+36del
ENST00000403106.7:c.180+33_180+36del	ENSP00000385981.3:n.180+33_180+36del
ENST00000622532.1:c.180+33_180+36del	ENSP00000478487.1:n.180+33_180+36del
NM_000508.3:c.180+33_180+36del , LRG_557t1:c.180+33_180+36del	NP_000499.1:n.180+33_180+36del
NM_021871.2:c.180+33_180+36del , LRG_557t2:c.180+33_180+36del	NP_068657.1:n.180+33_180+36del
NM_000508.4:c.180+33_180+36del	NP_000499.1:n.180+33_180+36del
NM_021871.3:c.180+33_180+36del	NP_068657.1:n.180+33_180+36del
NM_021871.4:c.180+33_180+36del MANE Select	NP_068657.1:n.180+33_180+36del
NM_000508.5:c.180+33_180+36del	NP_000499.1:n.180+33_180+36del