Canonical Allele Identifier: CA1406373028

Gene: SPSB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080366G= , CM000665.2:g.141080366G=	GRCh38
NC_000003.11:g.140799208G= , CM000665.1:g.140799208G=	GRCh37
NC_000003.10:g.142281898G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13568G= MANE Select	ENSP00000311609.2:n.694+13568G=
ENST00000310546.2:c.694+13568G=	ENSP00000311609.2:n.694+13568G=
ENST00000507895.1:n.215G=
ENST00000508126.1:c.161+13568G=
ENST00000508828.1:n.530G=
NM_080862.2:c.694+13568G=	NP_543138.1:n.694+13568G=
XM_011513313.1:c.694+13568G=	XP_011511615.1:n.694+13568G=
XR_924215.1:n.1505G=
XR_924216.1:n.1505G=
XM_017007509.2:c.*69G=	XP_016862998.1:n.*69G=
XR_924215.3:n.986G=
XR_924216.3:n.986G=
NM_080862.3:c.694+13568G= MANE Select	NP_543138.1:n.694+13568G=