Canonical Allele Identifier: CA350657258

Gene: STK36

Linked Data

• MyVariant Identifiers: chr2:g.219545327G>A (hg19) ; chr2:g.218680604G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218680604G>A , CM000664.2:g.218680604G>A	GRCh38
NC_000002.11:g.219545327G>A , CM000664.1:g.219545327G>A	GRCh37
NC_000002.10:g.219253571G>A	NCBI36
NG_029739.1:g.13579G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295709.8:c.1138G>A MANE Select	ENSP00000295709.3:p.Glu380Lys
ENST00000295709.7:c.1138G>A	ENSP00000295709.3:p.Glu380Lys
ENST00000392105.7:c.1138G>A	ENSP00000375954.3:p.Glu380Lys
ENST00000414413.5:c.33G>A
ENST00000440309.5:c.1138G>A	ENSP00000394095.1:p.Glu380Lys
NM_001243313.1:c.1138G>A	NP_001230242.1:p.Glu380Lys
NM_015690.4:c.1138G>A	NP_056505.2:p.Glu380Lys
XM_005246464.1:c.1138G>A	XP_005246521.1:p.Glu380Lys
XM_011510959.1:c.1138G>A	XP_011509261.1:p.Glu380Lys
XM_011510960.1:c.976G>A	XP_011509262.1:p.Glu326Lys
XR_922904.1:n.1417G>A
XM_005246464.2:c.1138G>A	XP_005246521.1:p.Glu380Lys
XM_011510959.2:c.1138G>A	XP_011509261.1:p.Glu380Lys
XM_017003804.2:c.1138G>A	XP_016859293.1:p.Glu380Lys
XM_017003805.2:c.-559G>A	XP_016859294.1:n.-559G>A
XR_001738704.2:n.1394G>A
XR_922904.2:n.1394G>A
NM_015690.5:c.1138G>A MANE Select	NP_056505.2:p.Glu380Lys
NM_001243313.2:c.1138G>A	NP_001230242.1:p.Glu380Lys
NM_001369423.1:c.1138G>A	NP_001356352.1:p.Glu380Lys