Canonical Allele Identifier: CA1406372986
Gene: SPSB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.141080273T= , CM000665.2:g.141080273T= GRCh38
NC_000003.11:g.140799115T= , CM000665.1:g.140799115T= GRCh37
NC_000003.10:g.142281805T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310546.3:c.694+13475T= MANE Select ENSP00000311609.2:n.694+13475T=
ENST00000310546.2:c.694+13475T= ENSP00000311609.2:n.694+13475T=
ENST00000507895.1:n.139-17T=
ENST00000508126.1:c.161+13475T=
ENST00000508828.1:n.454-17T=
NM_080862.2:c.694+13475T= NP_543138.1:n.694+13475T=
XM_011513313.1:c.694+13475T= XP_011511615.1:n.694+13475T=
XR_924215.1:n.1429-17T=
XR_924216.1:n.1429-17T=
XM_017007509.2:c.695-17T= XP_016862998.1:n.695-17T=
XR_924215.3:n.910-17T=
XR_924216.3:n.910-17T=
NM_080862.3:c.694+13475T= MANE Select NP_543138.1:n.694+13475T=