Canonical Allele Identifier: CA1310481972
Gene: PJVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178456113C= , CM000664.2:g.178456113C= GRCh38
NC_000002.11:g.179320840C= , CM000664.1:g.179320840C= GRCh37
NC_000002.10:g.179029086C= NCBI36
NG_009053.1:g.119G=
NG_012186.1:g.9678C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642192.1:c.34C= ENSP00000494225.1:p.Leu12=
ENST00000642492.1:c.34C= ENSP00000496267.1:p.Leu12=
ENST00000643738.1:c.34C= ENSP00000493684.1:p.Leu12=
ENST00000643768.1:n.168C=
ENST00000644580.2:c.511C= MANE Select ENSP00000495855.2:p.Leu171=
ENST00000645572.1:c.511C= ENSP00000494301.1:p.Leu171=
ENST00000645762.1:n.625C=
ENST00000645817.1:c.34C= ENSP00000495731.1:p.Leu12=
ENST00000647226.1:c.34C= ENSP00000496024.1:p.Leu12=
ENST00000375129.8:c.511C= ENSP00000364271.4:p.Leu171=
ENST00000409117.7:c.511C= ENSP00000386647.3:p.Leu171=
ENST00000437056.5:n.1381C=
ENST00000442710.5:c.353C=
ENST00000444615.1:c.153C=
NM_001042702.3:c.511C= NP_001036167.1:p.Leu171=
XM_005246627.1:c.520C= XP_005246684.1:p.Leu174=
XM_005246628.2:c.616C= XP_005246685.1:p.Leu206=
XM_005246629.2:c.502C= XP_005246686.1:p.Leu168=
XM_011511247.1:c.616C= XP_011509549.1:p.Leu206=
XM_011511248.1:c.580C= XP_011509550.1:p.Leu194=
XM_011511249.1:c.34C= XP_011509551.1:p.Leu12=
XM_011511250.1:c.34C= XP_011509552.1:p.Leu12=
XM_011511251.1:c.34C= XP_011509553.1:p.Leu12=
XR_922929.1:n.1283C=
NM_001042702.4:c.511C= NP_001036167.1:p.Leu171=
NM_001353775.1:c.520C= NP_001340704.1:p.Leu174=
NM_001353776.1:c.616C= NP_001340705.1:p.Leu206=
NM_001353777.1:c.34C= NP_001340706.1:p.Leu12=
NM_001353778.1:c.34C= NP_001340707.1:p.Leu12=
XM_005246629.4:c.502C= XP_005246686.1:p.Leu168=
XM_011511247.3:c.616C= XP_011509549.1:p.Leu206=
XM_011511249.3:c.34C= XP_011509551.1:p.Leu12=
XM_017004221.2:c.616C= XP_016859710.1:p.Leu206=
XM_017004224.2:c.34C= XP_016859713.1:p.Leu12=
XM_024452927.1:c.34C= XP_024308695.1:p.Leu12=
XM_024452928.1:c.34C= XP_024308696.1:p.Leu12=
XR_001738753.2:n.2323C=
XR_002959300.1:n.2323C=
XR_922929.3:n.806C=
NM_001042702.5:c.511C= MANE Select NP_001036167.1:p.Leu171=
NM_001369912.1:c.511C= NP_001356841.1:p.Leu171=
NM_001353775.2:c.520C= NP_001340704.1:p.Leu174=
NM_001353776.2:c.616C= NP_001340705.1:p.Leu206=
NM_001353778.2:c.34C= NP_001340707.1:p.Leu12=