Canonical Allele Identifier: CA1310480927
Gene: PJVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178453591T= , CM000664.2:g.178453591T= GRCh38
NC_000002.11:g.179318318T= , CM000664.1:g.179318318T= GRCh37
NC_000002.10:g.179026564T= NCBI36
NG_009053.1:g.2641A=
NG_012186.1:g.7156T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642192.1:c.-296T= ENSP00000494225.1:n.-296T=
ENST00000642492.1:c.-397T= ENSP00000496267.1:n.-397T=
ENST00000643738.1:c.-296T= ENSP00000493684.1:n.-296T=
ENST00000644554.1:c.-296T= ENSP00000495037.1:n.-296T=
ENST00000644580.2:c.182T= MANE Select ENSP00000495855.2:p.Ile61=
ENST00000645572.1:c.182T= ENSP00000494301.1:p.Ile61=
ENST00000645762.1:n.296T=
ENST00000645817.1:c.-296T= ENSP00000495731.1:n.-296T=
ENST00000647226.1:c.-296T= ENSP00000496024.1:n.-296T=
ENST00000375129.8:c.182T= ENSP00000364271.4:p.Ile61=
ENST00000409117.7:c.182T= ENSP00000386647.3:p.Ile61=
ENST00000437056.5:n.341T=
ENST00000442710.5:c.24T=
NM_001042702.3:c.182T= NP_001036167.1:p.Ile61=
XM_005246627.1:c.191T= XP_005246684.1:p.Ile64=
XM_005246628.2:c.287T= XP_005246685.1:p.Ile96=
XM_005246629.2:c.173T= XP_005246686.1:p.Ile58=
XM_011511247.1:c.287T= XP_011509549.1:p.Ile96=
XM_011511248.1:c.251T= XP_011509550.1:p.Ile84=
XM_011511249.1:c.-266-741T= XP_011509551.1:n.-266-741T=
XM_011511250.1:c.-296T= XP_011509552.1:n.-296T=
XM_011511251.1:c.-266-741T= XP_011509553.1:n.-266-741T=
XR_922929.1:n.954T=
NM_001042702.4:c.182T= NP_001036167.1:p.Ile61=
NM_001353775.1:c.191T= NP_001340704.1:p.Ile64=
NM_001353776.1:c.287T= NP_001340705.1:p.Ile96=
NM_001353777.1:c.-296T= NP_001340706.1:n.-296T=
NM_001353778.1:c.-296T= NP_001340707.1:n.-296T=
XM_005246629.4:c.173T= XP_005246686.1:p.Ile58=
XM_011511247.3:c.287T= XP_011509549.1:p.Ile96=
XM_011511249.3:c.-266-741T= XP_011509551.1:n.-266-741T=
XM_017004221.2:c.287T= XP_016859710.1:p.Ile96=
XM_017004224.2:c.-1007T= XP_016859713.1:n.-1007T=
XM_024452927.1:c.-397T= XP_024308695.1:n.-397T=
XM_024452928.1:c.-296T= XP_024308696.1:n.-296T=
XR_001738753.2:n.1994T=
XR_002959300.1:n.1994T=
XR_922929.3:n.477T=
NM_001042702.5:c.182T= MANE Select NP_001036167.1:p.Ile61=
NM_001369912.1:c.182T= NP_001356841.1:p.Ile61=
NM_001353775.2:c.191T= NP_001340704.1:p.Ile64=
NM_001353776.2:c.287T= NP_001340705.1:p.Ile96=
NM_001353778.2:c.-296T= NP_001340707.1:n.-296T=