Canonical Allele Identifier: CA2575836657

Gene: FURIN

Linked Data

• gnomAD v4: 15-90881923-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90881928del , CM000677.2:g.90881928del	GRCh38
NC_000015.9:g.91425158del , CM000677.1:g.91425158del	GRCh37
NC_000015.8:g.89226162del	NCBI36
NG_029671.1:g.2471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268171.8:c.*50del MANE Select	ENSP00000268171.2:n.*50del
ENST00000680053.1:c.*50del	ENSP00000506143.1:n.*50del
ENST00000680086.1:n.323+191del
ENST00000680687.1:c.*1659del	ENSP00000505177.1:n.*1659del
ENST00000681804.1:c.*1795del	ENSP00000505828.1:n.*1795del
ENST00000681865.1:c.*50del	ENSP00000505303.1:n.*50del
ENST00000268171.7:c.*50del	ENSP00000268171.2:n.*50del
ENST00000610579.4:c.*50del	ENSP00000484952.1:n.*50del
ENST00000618099.4:c.*50del	ENSP00000483552.1:n.*50del
NM_001289823.1:c.*50del	NP_001276752.1:n.*50del
NM_001289824.1:c.*50del	NP_001276753.1:n.*50del
NM_002569.3:c.*50del	NP_002560.1:n.*50del
NM_002569.4:c.*50del MANE Select	NP_002560.1:n.*50del
NM_001289823.2:c.*50del	NP_001276752.1:n.*50del
NM_001289824.2:c.*50del	NP_001276753.1:n.*50del
NM_001382619.1:c.*50del	NP_001369548.1:n.*50del
NM_001382620.1:c.*50del	NP_001369549.1:n.*50del
NM_001382621.1:c.*50del	NP_001369550.1:n.*50del
NM_001382622.1:c.*466del	NP_001369551.1:n.*466del
NR_168464.1:n.2658del