Canonical Allele Identifier: CA1406372955

Gene: SPSB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080192_141080193delinsGC , CM000665.2:g.141080192_141080193delinsGC	GRCh38
NC_000003.11:g.140799034_140799035delinsGC , CM000665.1:g.140799034_140799035delinsGC	GRCh37
NC_000003.10:g.142281724_142281725delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13394_694+13395delinsGC MANE Select	ENSP00000311609.2:n.694+13394_694+13395delinsGC
ENST00000310546.2:c.694+13394_694+13395delinsGC	ENSP00000311609.2:n.694+13394_694+13395delinsGC
ENST00000507895.1:n.139-98_139-97delinsGC
ENST00000508126.1:c.161+13394_161+13395delinsGC
ENST00000508828.1:n.454-98_454-97delinsGC
NM_080862.2:c.694+13394_694+13395delinsGC	NP_543138.1:n.694+13394_694+13395delinsGC
XM_011513313.1:c.694+13394_694+13395delinsGC	XP_011511615.1:n.694+13394_694+13395delinsGC
XR_924215.1:n.1429-98_1429-97delinsGC
XR_924216.1:n.1429-98_1429-97delinsGC
XM_017007509.2:c.695-98_695-97delinsGC	XP_016862998.1:n.695-98_695-97delinsGC
XR_924215.3:n.910-98_910-97delinsGC
XR_924216.3:n.910-98_910-97delinsGC
NM_080862.3:c.694+13394_694+13395delinsGC MANE Select	NP_543138.1:n.694+13394_694+13395delinsGC