Canonical Allele Identifier: CA1406372985
Gene: SPSB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.141080272G= , CM000665.2:g.141080272G= GRCh38
NC_000003.11:g.140799114G= , CM000665.1:g.140799114G= GRCh37
NC_000003.10:g.142281804G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310546.3:c.694+13474G= MANE Select ENSP00000311609.2:n.694+13474G=
ENST00000310546.2:c.694+13474G= ENSP00000311609.2:n.694+13474G=
ENST00000507895.1:n.139-18G=
ENST00000508126.1:c.161+13474G=
ENST00000508828.1:n.454-18G=
NM_080862.2:c.694+13474G= NP_543138.1:n.694+13474G=
XM_011513313.1:c.694+13474G= XP_011511615.1:n.694+13474G=
XR_924215.1:n.1429-18G=
XR_924216.1:n.1429-18G=
XM_017007509.2:c.695-18G= XP_016862998.1:n.695-18G=
XR_924215.3:n.910-18G=
XR_924216.3:n.910-18G=
NM_080862.3:c.694+13474G= MANE Select NP_543138.1:n.694+13474G=