Canonical Allele Identifier: CA1328870953
Gene: STK36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218680591T= , CM000664.2:g.218680591T= GRCh38
NC_000002.11:g.219545314T= , CM000664.1:g.219545314T= GRCh37
NC_000002.10:g.219253558T= NCBI36
NG_029739.1:g.13566T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295709.8:c.1137-12T= MANE Select ENSP00000295709.3:n.1137-12T=
ENST00000295709.7:c.1137-12T= ENSP00000295709.3:n.1137-12T=
ENST00000392105.7:c.1137-12T= ENSP00000375954.3:n.1137-12T=
ENST00000414413.5:c.32-12T=
ENST00000440309.5:c.1137-12T= ENSP00000394095.1:n.1137-12T=
NM_001243313.1:c.1137-12T= NP_001230242.1:n.1137-12T=
NM_015690.4:c.1137-12T= NP_056505.2:n.1137-12T=
XM_005246464.1:c.1137-12T= XP_005246521.1:n.1137-12T=
XM_011510959.1:c.1137-12T= XP_011509261.1:n.1137-12T=
XM_011510960.1:c.975-12T= XP_011509262.1:n.975-12T=
XR_922904.1:n.1416-12T=
XM_005246464.2:c.1137-12T= XP_005246521.1:n.1137-12T=
XM_011510959.2:c.1137-12T= XP_011509261.1:n.1137-12T=
XM_017003804.2:c.1137-12T= XP_016859293.1:n.1137-12T=
XM_017003805.2:c.-560-12T= XP_016859294.1:n.-560-12T=
XR_001738704.2:n.1393-12T=
XR_922904.2:n.1393-12T=
NM_015690.5:c.1137-12T= MANE Select NP_056505.2:n.1137-12T=
NM_001243313.2:c.1137-12T= NP_001230242.1:n.1137-12T=
NM_001369423.1:c.1137-12T= NP_001356352.1:n.1137-12T=