Canonical Allele Identifier: CA899796039

Gene: SPSB4

Linked Data

• dbSNP Id: rs1349959324
• MyVariant Identifiers: chr3:g.140799149del (hg19) ; chr3:g.141080307del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080311del , CM000665.2:g.141080311del	GRCh38
NC_000003.11:g.140799153del , CM000665.1:g.140799153del	GRCh37
NC_000003.10:g.142281843del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13513del MANE Select	ENSP00000311609.2:n.694+13513del
ENST00000310546.2:c.694+13513del	ENSP00000311609.2:n.694+13513del
ENST00000507895.1:n.160del
ENST00000508126.1:c.161+13513del
ENST00000508828.1:n.475del
NM_080862.2:c.694+13513del	NP_543138.1:n.694+13513del
XM_011513313.1:c.694+13513del	XP_011511615.1:n.694+13513del
XR_924215.1:n.1450del
XR_924216.1:n.1450del
XM_017007509.2:c.*14del	XP_016862998.1:n.*14del
XR_924215.3:n.931del
XR_924216.3:n.931del
NM_080862.3:c.694+13513del MANE Select	NP_543138.1:n.694+13513del