Canonical Allele Identifier: CA1406373041
Gene: SPSB4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.141080392A= , CM000665.2:g.141080392A= GRCh38
NC_000003.11:g.140799234A= , CM000665.1:g.140799234A= GRCh37
NC_000003.10:g.142281924A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310546.3:c.694+13594A= MANE Select ENSP00000311609.2:n.694+13594A=
ENST00000310546.2:c.694+13594A= ENSP00000311609.2:n.694+13594A=
ENST00000507895.1:n.241A=
ENST00000508126.1:c.161+13594A=
NM_080862.2:c.694+13594A= NP_543138.1:n.694+13594A=
XM_011513313.1:c.694+13594A= XP_011511615.1:n.694+13594A=
XR_924215.1:n.1531A=
XR_924216.1:n.1531A=
XM_017007509.2:c.*95A= XP_016862998.1:n.*95A=
XR_924215.3:n.1012A=
XR_924216.3:n.1012A=
NM_080862.3:c.694+13594A= MANE Select NP_543138.1:n.694+13594A=
Search 100 bp 5'
Search 100 bp 3'