Canonical Allele Identifier: CA1406372949

Gene: SPSB4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080183T= , CM000665.2:g.141080183T=	GRCh38
NC_000003.11:g.140799025T= , CM000665.1:g.140799025T=	GRCh37
NC_000003.10:g.142281715T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13385T= MANE Select	ENSP00000311609.2:n.694+13385T=
ENST00000310546.2:c.694+13385T=	ENSP00000311609.2:n.694+13385T=
ENST00000507895.1:n.139-107T=
ENST00000508126.1:c.161+13385T=
ENST00000508828.1:n.454-107T=
NM_080862.2:c.694+13385T=	NP_543138.1:n.694+13385T=
XM_011513313.1:c.694+13385T=	XP_011511615.1:n.694+13385T=
XR_924215.1:n.1429-107T=
XR_924216.1:n.1429-107T=
XM_017007509.2:c.695-107T=	XP_016862998.1:n.695-107T=
XR_924215.3:n.910-107T=
XR_924216.3:n.910-107T=
NM_080862.3:c.694+13385T= MANE Select	NP_543138.1:n.694+13385T=