Canonical Allele Identifier: CA2758665010

Gene: SPSB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080332_141080336del , CM000665.2:g.141080332_141080336del	GRCh38
NC_000003.11:g.140799174_140799178del , CM000665.1:g.140799174_140799178del	GRCh37
NC_000003.10:g.142281864_142281868del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13534_694+13538del MANE Select	ENSP00000311609.2:n.694+13534_694+13538del
ENST00000310546.2:c.694+13534_694+13538del	ENSP00000311609.2:n.694+13534_694+13538del
ENST00000507895.1:n.181_185del
ENST00000508126.1:c.161+13534_161+13538del
ENST00000508828.1:n.496_500del
NM_080862.2:c.694+13534_694+13538del	NP_543138.1:n.694+13534_694+13538del
XM_011513313.1:c.694+13534_694+13538del	XP_011511615.1:n.694+13534_694+13538del
XR_924215.1:n.1471_1475del
XR_924216.1:n.1471_1475del
XM_017007509.2:c.*35_*39del	XP_016862998.1:n.*35_*39del
XR_924215.3:n.952_956del
XR_924216.3:n.952_956del
NM_080862.3:c.694+13534_694+13538del MANE Select	NP_543138.1:n.694+13534_694+13538del