Canonical Allele Identifier: CA1406373050
Gene: SPSB4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.141080408G= , CM000665.2:g.141080408G= GRCh38
NC_000003.11:g.140799250G= , CM000665.1:g.140799250G= GRCh37
NC_000003.10:g.142281940G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310546.3:c.694+13610G= MANE Select ENSP00000311609.2:n.694+13610G=
ENST00000310546.2:c.694+13610G= ENSP00000311609.2:n.694+13610G=
ENST00000507895.1:n.257G=
ENST00000508126.1:c.161+13610G=
NM_080862.2:c.694+13610G= NP_543138.1:n.694+13610G=
XM_011513313.1:c.694+13610G= XP_011511615.1:n.694+13610G=
XR_924215.1:n.1547G=
XR_924216.1:n.1547G=
XM_017007509.2:c.*111G= XP_016862998.1:n.*111G=
XR_924215.3:n.1028G=
XR_924216.3:n.1028G=
NM_080862.3:c.694+13610G= MANE Select NP_543138.1:n.694+13610G=
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