Canonical Allele Identifier: CA1406372956

Gene: SPSB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080193C= , CM000665.2:g.141080193C=	GRCh38
NC_000003.11:g.140799035C= , CM000665.1:g.140799035C=	GRCh37
NC_000003.10:g.142281725C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310546.3:c.694+13395C= MANE Select	ENSP00000311609.2:n.694+13395C=
ENST00000310546.2:c.694+13395C=	ENSP00000311609.2:n.694+13395C=
ENST00000507895.1:n.139-97C=
ENST00000508126.1:c.161+13395C=
ENST00000508828.1:n.454-97C=
NM_080862.2:c.694+13395C=	NP_543138.1:n.694+13395C=
XM_011513313.1:c.694+13395C=	XP_011511615.1:n.694+13395C=
XR_924215.1:n.1429-97C=
XR_924216.1:n.1429-97C=
XM_017007509.2:c.695-97C=	XP_016862998.1:n.695-97C=
XR_924215.3:n.910-97C=
XR_924216.3:n.910-97C=
NM_080862.3:c.694+13395C= MANE Select	NP_543138.1:n.694+13395C=