Canonical Allele Identifier: CA26507827

Gene: PKN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.88754789G>A , CM000663.2:g.88754789G>A	GRCh38
NC_000001.10:g.89220472G>A , CM000663.1:g.89220472G>A	GRCh37
NC_000001.9:g.88993060G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370521.8:c.350-5433G>A MANE Select	ENSP00000359552.3:n.350-5433G>A
ENST00000316005.11:c.350-5433G>A	ENSP00000317851.7:n.350-5433G>A
ENST00000370505.7:c.-122-5433G>A	ENSP00000359536.5:n.-122-5433G>A
ENST00000370513.9:c.350-5433G>A	ENSP00000359544.5:n.350-5433G>A
ENST00000370521.7:c.350-5433G>A	ENSP00000359552.3:n.350-5433G>A
NM_006256.2:c.350-5433G>A	NP_006247.1:n.350-5433G>A
XM_005271031.1:c.350-5433G>A	XP_005271088.1:n.350-5433G>A
XM_011541769.1:c.431-5433G>A	XP_011540071.1:n.431-5433G>A
XM_011541770.1:c.431-5433G>A	XP_011540072.1:n.431-5433G>A
XM_011541771.1:c.431-5433G>A	XP_011540073.1:n.431-5433G>A
NM_001320707.1:c.350-5433G>A	NP_001307636.1:n.350-5433G>A
NM_001320708.1:c.-122-5433G>A	NP_001307637.1:n.-122-5433G>A
NM_001320709.1:c.350-5433G>A	NP_001307638.1:n.350-5433G>A
NM_006256.3:c.350-5433G>A	NP_006247.1:n.350-5433G>A
XM_017001782.2:c.350-5433G>A	XP_016857271.1:n.350-5433G>A
XM_017001783.2:c.350-5433G>A	XP_016857272.1:n.350-5433G>A
NM_006256.4:c.350-5433G>A MANE Select	NP_006247.1:n.350-5433G>A
NM_001320708.2:c.-122-5433G>A	NP_001307637.1:n.-122-5433G>A
NM_001320709.2:c.350-5433G>A	NP_001307638.1:n.350-5433G>A
NM_001320707.2:c.350-5433G>A	NP_001307636.1:n.350-5433G>A