Canonical Allele Identifier: CA2111069

Gene: STK36

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218693975G>A , CM000664.2:g.218693975G>A	GRCh38
NC_000002.11:g.219558698G>A , CM000664.1:g.219558698G>A	GRCh37
NC_000002.10:g.219266942G>A	NCBI36
NG_029739.1:g.26950G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015690.5:c.2328G>A MANE Select	NP_056505.2:p.Leu776=
ENST00000295709.8:c.2328G>A MANE Select	ENSP00000295709.3:p.Leu776=
NM_001243313.1:c.2328G>A	NP_001230242.1:p.Leu776=
NM_001243313.2:c.2328G>A	NP_001230242.1:p.Leu776=
NM_001369423.1:c.2328G>A	NP_001356352.1:p.Leu776=
NM_015690.4:c.2328G>A	NP_056505.2:p.Leu776=
ENST00000295709.7:c.2328G>A	ENSP00000295709.3:p.Leu776=
ENST00000392105.7:c.2328G>A	ENSP00000375954.3:p.Leu776=
ENST00000440309.5:c.2328G>A	ENSP00000394095.1:p.Leu776=
ENST00000486644.1:n.229G>A
ENST00000492486.5:n.569G>A
XM_005246464.1:c.2328G>A	XP_005246521.1:p.Leu776=
XM_005246464.2:c.2328G>A	XP_005246521.1:p.Leu776=
XM_011510959.1:c.2301G>A	XP_011509261.1:p.Leu767=
XM_011510959.2:c.2301G>A	XP_011509261.1:p.Leu767=
XM_011510960.1:c.2166G>A	XP_011509262.1:p.Leu722=
XM_011510961.1:c.735G>A	XP_011509263.1:p.Leu245=
XM_017003804.2:c.2328G>A	XP_016859293.1:p.Leu776=
XM_017003805.2:c.735G>A	XP_016859294.1:p.Leu245=
XR_001738704.2:n.2609G>A
XR_922904.1:n.2607G>A
XR_922904.2:n.2584G>A