Canonical Allele Identifier: CA1406373036

Gene: SPSB4

Linked Data

• dbSNP Id: rs1938207850

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080380_141080381del , CM000665.2:g.141080380_141080381del	GRCh38
NC_000003.11:g.140799222_140799223del , CM000665.1:g.140799222_140799223del	GRCh37
NC_000003.10:g.142281912_142281913del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310546.3:c.694+13582_694+13583del MANE Select	ENSP00000311609.2:n.694+13582_694+13583de...
ENST00000310546.2:c.694+13582_694+13583del	ENSP00000311609.2:n.694+13582_694+13583de...
ENST00000507895.1:n.229_230del
ENST00000508126.1:c.161+13582_161+13583del
NM_080862.2:c.694+13582_694+13583del	NP_543138.1:n.694+13582_694+13583del
XM_011513313.1:c.694+13582_694+13583del	XP_011511615.1:n.694+13582_694+13583del
XR_924215.1:n.1519_1520del
XR_924216.1:n.1519_1520del
XM_017007509.2:c.*83_*84del	XP_016862998.1:n.*83_*84del
XR_924215.3:n.1000_1001del
XR_924216.3:n.1000_1001del
NM_080862.3:c.694+13582_694+13583del MANE Select	NP_543138.1:n.694+13582_694+13583del