Canonical Allele Identifier: CA2630387183

Gene: FURIN

Linked Data

• gnomAD v4: 15-90881919-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90881919G>A , CM000677.2:g.90881919G>A	GRCh38
NC_000015.9:g.91425149G>A , CM000677.1:g.91425149G>A	GRCh37
NC_000015.8:g.89226153G>A	NCBI36
NG_029671.1:g.2462G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268171.8:c.*41G>A MANE Select	ENSP00000268171.2:n.*41G>A
ENST00000680053.1:c.*41G>A	ENSP00000506143.1:n.*41G>A
ENST00000680086.1:n.323+182G>A
ENST00000680687.1:c.*1650G>A	ENSP00000505177.1:n.*1650G>A
ENST00000681804.1:c.*1786G>A	ENSP00000505828.1:n.*1786G>A
ENST00000681865.1:c.*41G>A	ENSP00000505303.1:n.*41G>A
ENST00000268171.7:c.*41G>A	ENSP00000268171.2:n.*41G>A
ENST00000610579.4:c.*41G>A	ENSP00000484952.1:n.*41G>A
ENST00000618099.4:c.*41G>A	ENSP00000483552.1:n.*41G>A
NM_001289823.1:c.*41G>A	NP_001276752.1:n.*41G>A
NM_001289824.1:c.*41G>A	NP_001276753.1:n.*41G>A
NM_002569.3:c.*41G>A	NP_002560.1:n.*41G>A
NM_002569.4:c.*41G>A MANE Select	NP_002560.1:n.*41G>A
NM_001289823.2:c.*41G>A	NP_001276752.1:n.*41G>A
NM_001289824.2:c.*41G>A	NP_001276753.1:n.*41G>A
NM_001382619.1:c.*41G>A	NP_001369548.1:n.*41G>A
NM_001382620.1:c.*41G>A	NP_001369549.1:n.*41G>A
NM_001382621.1:c.*41G>A	NP_001369550.1:n.*41G>A
NM_001382622.1:c.*457G>A	NP_001369551.1:n.*457G>A
NR_168464.1:n.2649G>A