Canonical Allele Identifier: CA2672444876

Gene: FGA

Linked Data

• gnomAD v4: 4-154585693-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154585694_154585695del , CM000666.2:g.154585694_154585695del	GRCh38
NC_000004.11:g.155506846_155506847del , CM000666.1:g.155506846_155506847del	GRCh37
NC_000004.10:g.155726296_155726297del	NCBI36
NG_008832.1:g.10051_10052del , LRG_557:g.10051_10052del

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.1734_1735del	ENSP00000498441.1:p.Ser578ArgfsTer7
ENST00000403106.8:c.1734_1735del MANE Select	ENSP00000385981.3:p.Ser578ArgfsTer7
ENST00000651975.1:c.1734_1735del	ENSP00000498441.1:p.Ser578ArgfsTer7
ENST00000302053.7:c.1734_1735del	ENSP00000306361.3:p.Ser578ArgfsTer7
ENST00000403106.7:c.1734_1735del	ENSP00000385981.3:p.Ser578ArgfsTer7
ENST00000622532.1:c.659_660del	ENSP00000478487.1:p.Val220AspfsTer?
NM_000508.3:c.1734_1735del , LRG_557t1:c.1734_1735del	NP_000499.1:p.Ser578ArgfsTer7
NM_021871.2:c.1734_1735del , LRG_557t2:c.1734_1735del	NP_068657.1:p.Ser578ArgfsTer7
NM_000508.4:c.1734_1735del	NP_000499.1:p.Ser578ArgfsTer7
NM_021871.3:c.1734_1735del	NP_068657.1:p.Ser578ArgfsTer7
NM_021871.4:c.1734_1735del MANE Select	NP_068657.1:p.Ser578ArgfsTer7
NM_000508.5:c.1734_1735del	NP_000499.1:p.Ser578ArgfsTer7