Canonical Allele Identifier: CA349296735

Gene: PDK1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.172558729A>C , CM000664.2:g.172558729A>C	GRCh38
NC_000002.11:g.173423457A>C , CM000664.1:g.173423457A>C	GRCh37
NC_000002.10:g.173131703A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002610.5:c.218A>C MANE Select	NP_002601.1:p.Lys73Thr
ENST00000282077.8:c.218A>C MANE Select	ENSP00000282077.3:p.Lys73Thr
NM_001278549.1:c.218A>C	NP_001265478.1:p.Lys73Thr
NM_001278549.2:c.218A>C	NP_001265478.1:p.Lys73Thr
NM_002610.4:c.218A>C	NP_002601.1:p.Lys73Thr
NR_103729.1:n.400A>C
NR_103729.2:n.279A>C
NR_103731.1:n.369A>C
ENST00000282077.7:c.218A>C	ENSP00000282077.2:p.Lys73Thr
ENST00000392571.6:c.218A>C	ENSP00000376352.2:p.Lys73Thr
ENST00000410055.5:c.218A>C	ENSP00000386985.1:p.Lys73Thr
ENST00000416991.5:c.44A>C	ENSP00000399160.1:p.Lys15Thr
ENST00000431718.5:c.218A>C	ENSP00000413629.1:p.Lys73Thr
ENST00000436490.5:c.-11A>C	ENSP00000406608.1:n.-11A>C
ENST00000439519.1:c.-11A>C	ENSP00000388366.1:n.-11A>C
ENST00000443353.5:c.-11A>C	ENSP00000399558.1:n.-11A>C
XM_006712594.2:c.218A>C	XP_006712657.1:p.Lys73Thr
XM_011511343.1:c.-11A>C	XP_011509645.1:n.-11A>C
XM_011511343.2:c.-11A>C	XP_011509645.1:n.-11A>C
XM_011511344.1:c.-11A>C	XP_011509646.1:n.-11A>C
XM_011511344.2:c.-11A>C	XP_011509646.1:n.-11A>C
XM_011511345.1:c.-11A>C	XP_011509647.1:n.-11A>C
XM_011511345.3:c.-11A>C	XP_011509647.1:n.-11A>C
XM_011511346.1:c.218A>C	XP_011509648.1:p.Lys73Thr
XM_011511347.1:c.-11A>C	XP_011509649.1:n.-11A>C
XM_011511347.2:c.-11A>C	XP_011509649.1:n.-11A>C
XR_001738771.1:n.279A>C
XR_001738772.2:n.279A>C
XR_001738773.1:n.279A>C
XR_001738774.2:n.291A>C
XR_001738775.2:n.291A>C
XR_001738776.1:n.279A>C
XR_427093.1:n.279A>C
XR_427093.3:n.279A>C
XR_427094.1:n.279A>C
XR_427095.1:n.295A>C
XR_427095.3:n.291A>C
XR_922942.1:n.279A>C
XR_922942.2:n.279A>C
XR_922943.1:n.279A>C
XR_922943.2:n.279A>C
XR_922944.1:n.279A>C
XR_922944.2:n.279A>C
XR_922945.1:n.279A>C
XR_922946.1:n.279A>C