Canonical Allele Identifier: CA1435124947

Gene: STK32B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5083198T= , CM000666.2:g.5083198T=	GRCh38
NC_000004.11:g.5084925T= , CM000666.1:g.5084925T=	GRCh37
NC_000004.10:g.5135826T=	NCBI36
NG_051593.1:g.36876T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282908.10:c.52+31283T= MANE Select	ENSP00000282908.5:n.52+31283T=
ENST00000282908.9:c.52+31283T=	ENSP00000282908.5:n.52+31283T=
ENST00000512018.5:c.52+31283T=	ENSP00000422820.1:n.52+31283T=
NM_001306082.1:c.-200+31283T=	NP_001293011.1:n.-200+31283T=
NM_018401.1:c.52+31283T=	NP_060871.1:n.52+31283T=
NM_018401.2:c.52+31283T=	NP_060871.1:n.52+31283T=
XM_011513497.1:c.52+31283T=	XP_011511799.1:n.52+31283T=
XM_011513498.1:c.52+31283T=	XP_011511800.1:n.52+31283T=
XM_011513499.1:c.52+31283T=	XP_011511801.1:n.52+31283T=
XM_011513500.1:c.52+31283T=	XP_011511802.1:n.52+31283T=
XM_011513502.1:c.52+31283T=	XP_011511804.1:n.52+31283T=
NM_001345969.1:c.52+31283T=	NP_001332898.1:n.52+31283T=
NM_018401.3:c.52+31283T= MANE Select	NP_060871.1:n.52+31283T=
NM_001306082.2:c.-200+31283T=	NP_001293011.1:n.-200+31283T=
NM_001345969.2:c.52+31283T=	NP_001332898.1:n.52+31283T=