Canonical Allele Identifier: CA1328870954
Gene: STK36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218680593C= , CM000664.2:g.218680593C= GRCh38
NC_000002.11:g.219545316C= , CM000664.1:g.219545316C= GRCh37
NC_000002.10:g.219253560C= NCBI36
NG_029739.1:g.13568C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295709.8:c.1137-10C= MANE Select ENSP00000295709.3:n.1137-10C=
ENST00000295709.7:c.1137-10C= ENSP00000295709.3:n.1137-10C=
ENST00000392105.7:c.1137-10C= ENSP00000375954.3:n.1137-10C=
ENST00000414413.5:c.32-10C=
ENST00000440309.5:c.1137-10C= ENSP00000394095.1:n.1137-10C=
NM_001243313.1:c.1137-10C= NP_001230242.1:n.1137-10C=
NM_015690.4:c.1137-10C= NP_056505.2:n.1137-10C=
XM_005246464.1:c.1137-10C= XP_005246521.1:n.1137-10C=
XM_011510959.1:c.1137-10C= XP_011509261.1:n.1137-10C=
XM_011510960.1:c.975-10C= XP_011509262.1:n.975-10C=
XR_922904.1:n.1416-10C=
XM_005246464.2:c.1137-10C= XP_005246521.1:n.1137-10C=
XM_011510959.2:c.1137-10C= XP_011509261.1:n.1137-10C=
XM_017003804.2:c.1137-10C= XP_016859293.1:n.1137-10C=
XM_017003805.2:c.-560-10C= XP_016859294.1:n.-560-10C=
XR_001738704.2:n.1393-10C=
XR_922904.2:n.1393-10C=
NM_015690.5:c.1137-10C= MANE Select NP_056505.2:n.1137-10C=
NM_001243313.2:c.1137-10C= NP_001230242.1:n.1137-10C=
NM_001369423.1:c.1137-10C= NP_001356352.1:n.1137-10C=