Canonical Allele Identifier: CA1406373002

Gene: SPSB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080306_141080307delinsCT , CM000665.2:g.141080306_141080307delinsCT	GRCh38
NC_000003.11:g.140799148_140799149delinsCT , CM000665.1:g.140799148_140799149delinsCT	GRCh37
NC_000003.10:g.142281838_142281839delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13508_694+13509delinsCT MANE Select	ENSP00000311609.2:n.694+13508_694+13509delinsCT
ENST00000310546.2:c.694+13508_694+13509delinsCT	ENSP00000311609.2:n.694+13508_694+13509delinsCT
ENST00000507895.1:n.155_156delinsCT
ENST00000508126.1:c.161+13508_161+13509delinsCT
ENST00000508828.1:n.470_471delinsCT
NM_080862.2:c.694+13508_694+13509delinsCT	NP_543138.1:n.694+13508_694+13509delinsCT
XM_011513313.1:c.694+13508_694+13509delinsCT	XP_011511615.1:n.694+13508_694+13509delinsCT
XR_924215.1:n.1445_1446delinsCT
XR_924216.1:n.1445_1446delinsCT
XM_017007509.2:c.*9_*10delinsCT	XP_016862998.1:n.*9_*10delinsCT
XR_924215.3:n.926_927delinsCT
XR_924216.3:n.926_927delinsCT
NM_080862.3:c.694+13508_694+13509delinsCT MANE Select	NP_543138.1:n.694+13508_694+13509delinsCT