Canonical Allele Identifier: CA2630387388

Gene: FURIN

Linked Data

• gnomAD v4: 15-90881990-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90881990G>T , CM000677.2:g.90881990G>T	GRCh38
NC_000015.9:g.91425220G>T , CM000677.1:g.91425220G>T	GRCh37
NC_000015.8:g.89226224G>T	NCBI36
NG_029671.1:g.2533G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268171.8:c.*112G>T MANE Select	ENSP00000268171.2:n.*112G>T
ENST00000680053.1:c.*112G>T	ENSP00000506143.1:n.*112G>T
ENST00000680086.1:n.323+253G>T
ENST00000680687.1:c.*1721G>T	ENSP00000505177.1:n.*1721G>T
ENST00000681804.1:c.*1857G>T	ENSP00000505828.1:n.*1857G>T
ENST00000681865.1:c.*112G>T	ENSP00000505303.1:n.*112G>T
ENST00000268171.7:c.*112G>T	ENSP00000268171.2:n.*112G>T
ENST00000610579.4:c.*112G>T	ENSP00000484952.1:n.*112G>T
ENST00000618099.4:c.*112G>T	ENSP00000483552.1:n.*112G>T
NM_001289823.1:c.*112G>T	NP_001276752.1:n.*112G>T
NM_001289824.1:c.*112G>T	NP_001276753.1:n.*112G>T
NM_002569.3:c.*112G>T	NP_002560.1:n.*112G>T
NM_002569.4:c.*112G>T MANE Select	NP_002560.1:n.*112G>T
NM_001289823.2:c.*112G>T	NP_001276752.1:n.*112G>T
NM_001289824.2:c.*112G>T	NP_001276753.1:n.*112G>T
NM_001382619.1:c.*112G>T	NP_001369548.1:n.*112G>T
NM_001382620.1:c.*112G>T	NP_001369549.1:n.*112G>T
NM_001382621.1:c.*112G>T	NP_001369550.1:n.*112G>T
NM_001382622.1:c.*528G>T	NP_001369551.1:n.*528G>T
NR_168464.1:n.2720G>T