Canonical Allele Identifier: CA430080385

Gene: PJVK

Linked Data

• MyVariant Identifiers: chr2:g.179320794A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178456067A>G , CM000664.2:g.178456067A>G	GRCh38
NC_000002.11:g.179320794A>G , CM000664.1:g.179320794A>G	GRCh37
NC_000002.10:g.179029040A>G	NCBI36
NG_009053.1:g.165T>C
NG_012186.1:g.9632A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642192.1:c.-13A>G	ENSP00000494225.1:n.-13A>G
ENST00000642492.1:c.-13A>G	ENSP00000496267.1:n.-13A>G
ENST00000643738.1:c.-13A>G	ENSP00000493684.1:n.-13A>G
ENST00000643768.1:n.122A>G
ENST00000644554.1:c.-13A>G	ENSP00000495037.1:n.-13A>G
ENST00000644580.2:c.465A>G MANE Select	ENSP00000495855.2:p.Val155=
ENST00000645572.1:c.465A>G	ENSP00000494301.1:p.Val155=
ENST00000645762.1:n.579A>G
ENST00000645817.1:c.-13A>G	ENSP00000495731.1:n.-13A>G
ENST00000647226.1:c.-13A>G	ENSP00000496024.1:n.-13A>G
ENST00000375129.8:c.465A>G	ENSP00000364271.4:p.Val155=
ENST00000409117.7:c.465A>G	ENSP00000386647.3:p.Val155=
ENST00000437056.5:n.1335A>G
ENST00000442710.5:c.307A>G
ENST00000444615.1:c.107A>G
NM_001042702.3:c.465A>G	NP_001036167.1:p.Val155=
XM_005246627.1:c.474A>G	XP_005246684.1:p.Val158=
XM_005246628.2:c.570A>G	XP_005246685.1:p.Val190=
XM_005246629.2:c.456A>G	XP_005246686.1:p.Val152=
XM_011511247.1:c.570A>G	XP_011509549.1:p.Val190=
XM_011511248.1:c.534A>G	XP_011509550.1:p.Val178=
XM_011511249.1:c.-13A>G	XP_011509551.1:n.-13A>G
XM_011511250.1:c.-13A>G	XP_011509552.1:n.-13A>G
XM_011511251.1:c.-13A>G	XP_011509553.1:n.-13A>G
XR_922929.1:n.1237A>G
NM_001042702.4:c.465A>G	NP_001036167.1:p.Val155=
NM_001353775.1:c.474A>G	NP_001340704.1:p.Val158=
NM_001353776.1:c.570A>G	NP_001340705.1:p.Val190=
NM_001353777.1:c.-13A>G	NP_001340706.1:n.-13A>G
NM_001353778.1:c.-13A>G	NP_001340707.1:n.-13A>G
XM_005246629.4:c.456A>G	XP_005246686.1:p.Val152=
XM_011511247.3:c.570A>G	XP_011509549.1:p.Val190=
XM_011511249.3:c.-13A>G	XP_011509551.1:n.-13A>G
XM_017004221.2:c.570A>G	XP_016859710.1:p.Val190=
XM_017004224.2:c.-13A>G	XP_016859713.1:n.-13A>G
XM_024452927.1:c.-13A>G	XP_024308695.1:n.-13A>G
XM_024452928.1:c.-13A>G	XP_024308696.1:n.-13A>G
XR_001738753.2:n.2277A>G
XR_002959300.1:n.2277A>G
XR_922929.3:n.760A>G
NM_001042702.5:c.465A>G MANE Select	NP_001036167.1:p.Val155=
NM_001369912.1:c.465A>G	NP_001356841.1:p.Val155=
NM_001353775.2:c.474A>G	NP_001340704.1:p.Val158=
NM_001353776.2:c.570A>G	NP_001340705.1:p.Val190=
NM_001353778.2:c.-13A>G	NP_001340707.1:n.-13A>G