Canonical Allele Identifier: CA2667974490

Gene: SPSB4

Linked Data

• gnomAD v4: 3-141080279-CATTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080280_141080283del , CM000665.2:g.141080280_141080283del	GRCh38
NC_000003.11:g.140799122_140799125del , CM000665.1:g.140799122_140799125del	GRCh37
NC_000003.10:g.142281812_142281815del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13482_694+13485del MANE Select	ENSP00000311609.2:n.694+13482_694+13485del
ENST00000310546.2:c.694+13482_694+13485del	ENSP00000311609.2:n.694+13482_694+13485del
ENST00000507895.1:n.139-10_139-7del
ENST00000508126.1:c.161+13482_161+13485del
ENST00000508828.1:n.454-10_454-7del
NM_080862.2:c.694+13482_694+13485del	NP_543138.1:n.694+13482_694+13485del
XM_011513313.1:c.694+13482_694+13485del	XP_011511615.1:n.694+13482_694+13485del
XR_924215.1:n.1429-10_1429-7del
XR_924216.1:n.1429-10_1429-7del
XM_017007509.2:c.695-10_695-7del	XP_016862998.1:n.695-10_695-7del
XR_924215.3:n.910-10_910-7del
XR_924216.3:n.910-10_910-7del
NM_080862.3:c.694+13482_694+13485del MANE Select	NP_543138.1:n.694+13482_694+13485del