Canonical Allele Identifier: CA1310480928
Gene: PJVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178453593C= , CM000664.2:g.178453593C= GRCh38
NC_000002.11:g.179318320C= , CM000664.1:g.179318320C= GRCh37
NC_000002.10:g.179026566C= NCBI36
NG_009053.1:g.2639G=
NG_012186.1:g.7158C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642192.1:c.-294C= ENSP00000494225.1:n.-294C=
ENST00000642492.1:c.-395C= ENSP00000496267.1:n.-395C=
ENST00000643738.1:c.-294C= ENSP00000493684.1:n.-294C=
ENST00000644554.1:c.-294C= ENSP00000495037.1:n.-294C=
ENST00000644580.2:c.184C= MANE Select ENSP00000495855.2:p.Leu62=
ENST00000645572.1:c.184C= ENSP00000494301.1:p.Leu62=
ENST00000645762.1:n.298C=
ENST00000645817.1:c.-294C= ENSP00000495731.1:n.-294C=
ENST00000647226.1:c.-294C= ENSP00000496024.1:n.-294C=
ENST00000375129.8:c.184C= ENSP00000364271.4:p.Leu62=
ENST00000409117.7:c.184C= ENSP00000386647.3:p.Leu62=
ENST00000437056.5:n.343C=
ENST00000442710.5:c.26C=
NM_001042702.3:c.184C= NP_001036167.1:p.Leu62=
XM_005246627.1:c.193C= XP_005246684.1:p.Leu65=
XM_005246628.2:c.289C= XP_005246685.1:p.Leu97=
XM_005246629.2:c.175C= XP_005246686.1:p.Leu59=
XM_011511247.1:c.289C= XP_011509549.1:p.Leu97=
XM_011511248.1:c.253C= XP_011509550.1:p.Leu85=
XM_011511249.1:c.-266-739C= XP_011509551.1:n.-266-739C=
XM_011511250.1:c.-294C= XP_011509552.1:n.-294C=
XM_011511251.1:c.-266-739C= XP_011509553.1:n.-266-739C=
XR_922929.1:n.956C=
NM_001042702.4:c.184C= NP_001036167.1:p.Leu62=
NM_001353775.1:c.193C= NP_001340704.1:p.Leu65=
NM_001353776.1:c.289C= NP_001340705.1:p.Leu97=
NM_001353777.1:c.-294C= NP_001340706.1:n.-294C=
NM_001353778.1:c.-294C= NP_001340707.1:n.-294C=
XM_005246629.4:c.175C= XP_005246686.1:p.Leu59=
XM_011511247.3:c.289C= XP_011509549.1:p.Leu97=
XM_011511249.3:c.-266-739C= XP_011509551.1:n.-266-739C=
XM_017004221.2:c.289C= XP_016859710.1:p.Leu97=
XM_017004224.2:c.-1005C= XP_016859713.1:n.-1005C=
XM_024452927.1:c.-395C= XP_024308695.1:n.-395C=
XM_024452928.1:c.-294C= XP_024308696.1:n.-294C=
XR_001738753.2:n.1996C=
XR_002959300.1:n.1996C=
XR_922929.3:n.479C=
NM_001042702.5:c.184C= MANE Select NP_001036167.1:p.Leu62=
NM_001369912.1:c.184C= NP_001356841.1:p.Leu62=
NM_001353775.2:c.193C= NP_001340704.1:p.Leu65=
NM_001353776.2:c.289C= NP_001340705.1:p.Leu97=
NM_001353778.2:c.-294C= NP_001340707.1:n.-294C=