Canonical Allele Identifier: CA430077973

Gene: PJVK

Linked Data

• MyVariant Identifiers: chr2:g.179318346T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178453619T>G , CM000664.2:g.178453619T>G	GRCh38
NC_000002.11:g.179318346T>G , CM000664.1:g.179318346T>G	GRCh37
NC_000002.10:g.179026592T>G	NCBI36
NG_009053.1:g.2613A>C
NG_012186.1:g.7184T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642192.1:c.-268T>G	ENSP00000494225.1:n.-268T>G
ENST00000642492.1:c.-369T>G	ENSP00000496267.1:n.-369T>G
ENST00000643738.1:c.-268T>G	ENSP00000493684.1:n.-268T>G
ENST00000644554.1:c.-268T>G	ENSP00000495037.1:n.-268T>G
ENST00000644580.2:c.210T>G MANE Select	ENSP00000495855.2:p.Ala70=
ENST00000645572.1:c.210T>G	ENSP00000494301.1:p.Ala70=
ENST00000645762.1:n.324T>G
ENST00000645817.1:c.-268T>G	ENSP00000495731.1:n.-268T>G
ENST00000647226.1:c.-268T>G	ENSP00000496024.1:n.-268T>G
ENST00000375129.8:c.210T>G	ENSP00000364271.4:p.Ala70=
ENST00000409117.7:c.210T>G	ENSP00000386647.3:p.Ala70=
ENST00000437056.5:n.369T>G
ENST00000442710.5:c.52T>G
NM_001042702.3:c.210T>G	NP_001036167.1:p.Ala70=
XM_005246627.1:c.219T>G	XP_005246684.1:p.Ala73=
XM_005246628.2:c.315T>G	XP_005246685.1:p.Ala105=
XM_005246629.2:c.201T>G	XP_005246686.1:p.Ala67=
XM_011511247.1:c.315T>G	XP_011509549.1:p.Ala105=
XM_011511248.1:c.279T>G	XP_011509550.1:p.Ala93=
XM_011511249.1:c.-266-713T>G	XP_011509551.1:n.-266-713T>G
XM_011511250.1:c.-268T>G	XP_011509552.1:n.-268T>G
XM_011511251.1:c.-266-713T>G	XP_011509553.1:n.-266-713T>G
XR_922929.1:n.982T>G
NM_001042702.4:c.210T>G	NP_001036167.1:p.Ala70=
NM_001353775.1:c.219T>G	NP_001340704.1:p.Ala73=
NM_001353776.1:c.315T>G	NP_001340705.1:p.Ala105=
NM_001353777.1:c.-268T>G	NP_001340706.1:n.-268T>G
NM_001353778.1:c.-268T>G	NP_001340707.1:n.-268T>G
XM_005246629.4:c.201T>G	XP_005246686.1:p.Ala67=
XM_011511247.3:c.315T>G	XP_011509549.1:p.Ala105=
XM_011511249.3:c.-266-713T>G	XP_011509551.1:n.-266-713T>G
XM_017004221.2:c.315T>G	XP_016859710.1:p.Ala105=
XM_017004224.2:c.-979T>G	XP_016859713.1:n.-979T>G
XM_024452927.1:c.-369T>G	XP_024308695.1:n.-369T>G
XM_024452928.1:c.-268T>G	XP_024308696.1:n.-268T>G
XR_001738753.2:n.2022T>G
XR_002959300.1:n.2022T>G
XR_922929.3:n.505T>G
NM_001042702.5:c.210T>G MANE Select	NP_001036167.1:p.Ala70=
NM_001369912.1:c.210T>G	NP_001356841.1:p.Ala70=
NM_001353775.2:c.219T>G	NP_001340704.1:p.Ala73=
NM_001353776.2:c.315T>G	NP_001340705.1:p.Ala105=
NM_001353778.2:c.-268T>G	NP_001340707.1:n.-268T>G