Canonical Allele Identifier: CA60717102
Gene: PDK1 HGNC NCBI

Linked Data

dbSNP Id: rs11686903

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.172581558C>T , CM000664.2:g.172581558C>T GRCh38
NC_000002.11:g.173446286C>T , CM000664.1:g.173446286C>T GRCh37
NC_000002.10:g.173154532C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000282077.8:c.946-4720C>T MANE Select ENSP00000282077.3:n.946-4720C>T
ENST00000282077.7:c.946-4720C>T ENSP00000282077.2:n.946-4720C>T
ENST00000392571.6:c.1006-4720C>T ENSP00000376352.2:n.1006-4720C>T
ENST00000410055.5:c.946-4720C>T ENSP00000386985.1:n.946-4720C>T
ENST00000466437.1:n.241-4720C>T
NM_001278549.1:c.1006-4720C>T NP_001265478.1:n.1006-4720C>T
NM_002610.4:c.946-4720C>T NP_002601.1:n.946-4720C>T
NR_103729.1:n.1128-4720C>T
NR_103731.1:n.1097-4720C>T
XM_006712595.2:c.370-4720C>T XP_006712658.1:n.370-4720C>T
XM_011511343.1:c.778-4720C>T XP_011509645.1:n.778-4720C>T
XM_011511344.1:c.778-4720C>T XP_011509646.1:n.778-4720C>T
XM_011511345.1:c.718-4720C>T XP_011509647.1:n.718-4720C>T
XM_011511346.1:c.1006-3045C>T XP_011509648.1:n.1006-3045C>T
XM_011511347.1:c.778-4720C>T XP_011509649.1:n.778-4720C>T
XR_427093.1:n.1067-4720C>T
XR_427094.1:n.990-4720C>T
XR_427095.1:n.946-4720C>T
XR_922942.1:n.1067-4720C>T
XR_922943.1:n.1067-4720C>T
XR_922944.1:n.1067-4720C>T
XR_922945.1:n.1067-4720C>T
XR_922946.1:n.990-3045C>T
XM_006712595.3:c.370-4720C>T XP_006712658.1:n.370-4720C>T
XM_011511343.2:c.778-4720C>T XP_011509645.1:n.778-4720C>T
XM_011511344.2:c.778-4720C>T XP_011509646.1:n.778-4720C>T
XM_011511345.3:c.718-4720C>T XP_011509647.1:n.718-4720C>T
XM_011511347.2:c.778-4720C>T XP_011509649.1:n.778-4720C>T
XR_001738771.1:n.1067-4720C>T
XR_001738772.2:n.1067-4720C>T
XR_001738773.1:n.1067-4720C>T
XR_001738774.2:n.1019-4720C>T
XR_001738775.2:n.1019-4720C>T
XR_001738776.1:n.990-4720C>T
XR_427093.3:n.1067-4720C>T
XR_427095.3:n.942-4720C>T
XR_922942.2:n.1067-4720C>T
XR_922943.2:n.1067-4720C>T
XR_922944.2:n.1067-4720C>T
NM_001278549.2:c.1006-4720C>T NP_001265478.1:n.1006-4720C>T
NM_002610.5:c.946-4720C>T MANE Select NP_002601.1:n.946-4720C>T
NR_103729.2:n.1007-4720C>T