Canonical Allele Identifier: CA1589550981

Gene: STK32A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.147354035C= , CM000667.2:g.147354035C=	GRCh38
NC_000005.9:g.146733598C= , CM000667.1:g.146733598C=	GRCh37
NC_000005.8:g.146713791C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001112724.2:c.562+2881C= MANE Select	NP_001106195.1:n.562+2881C=
ENST00000397936.8:c.562+2881C= MANE Select	ENSP00000381030.3:n.562+2881C=
NM_001112724.1:c.562+2881C=	NP_001106195.1:n.562+2881C=
NM_001287740.1:c.562+2881C=	NP_001274669.1:n.562+2881C=
NM_001287740.2:c.562+2881C=	NP_001274669.1:n.562+2881C=
ENST00000306304.10:n.895+2881C=
ENST00000397936.7:c.562+2881C=	ENSP00000381030.3:n.562+2881C=
ENST00000398523.3:c.562+2881C=	ENSP00000381535.3:n.562+2881C=
ENST00000648628.1:c.556+2881C=	ENSP00000497167.1:n.556+2881C=
XM_011537576.1:c.556+2881C=	XP_011535878.1:n.556+2881C=
XM_011537577.1:c.562+2881C=	XP_011535879.1:n.562+2881C=
XM_011537577.2:c.562+2881C=	XP_011535879.1:n.562+2881C=
XM_011537578.1:c.562+2881C=	XP_011535880.1:n.562+2881C=
XM_011537579.1:c.562+2881C=	XP_011535881.1:n.562+2881C=
XM_011537579.2:c.562+2881C=	XP_011535881.1:n.562+2881C=
XM_017009213.1:c.562+2881C=	XP_016864702.1:n.562+2881C=
XM_017009214.1:c.55+2881C=	XP_016864703.1:n.55+2881C=
XR_001742037.1:n.895+2881C=
XR_001742038.1:n.895+2881C=