Canonical Allele Identifier: CA2667974491

Gene: SPSB4

Linked Data

• gnomAD v4: 3-141080281-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080281T>A , CM000665.2:g.141080281T>A	GRCh38
NC_000003.11:g.140799123T>A , CM000665.1:g.140799123T>A	GRCh37
NC_000003.10:g.142281813T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310546.3:c.694+13483T>A MANE Select	ENSP00000311609.2:n.694+13483T>A
ENST00000310546.2:c.694+13483T>A	ENSP00000311609.2:n.694+13483T>A
ENST00000507895.1:n.139-9T>A
ENST00000508126.1:c.161+13483T>A
ENST00000508828.1:n.454-9T>A
NM_080862.2:c.694+13483T>A	NP_543138.1:n.694+13483T>A
XM_011513313.1:c.694+13483T>A	XP_011511615.1:n.694+13483T>A
XR_924215.1:n.1429-9T>A
XR_924216.1:n.1429-9T>A
XM_017007509.2:c.695-9T>A	XP_016862998.1:n.695-9T>A
XR_924215.3:n.910-9T>A
XR_924216.3:n.910-9T>A
NM_080862.3:c.694+13483T>A MANE Select	NP_543138.1:n.694+13483T>A