Canonical Allele Identifier: CA2577169503

Gene: PJVK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178456101_178456102insA , CM000664.2:g.178456101_178456102insA	GRCh38
NC_000002.11:g.179320828_179320829insA , CM000664.1:g.179320828_179320829insA	GRCh37
NC_000002.10:g.179029074_179029075insA	NCBI36
NG_009053.1:g.130_131insT
NG_012186.1:g.9666_9667insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642192.1:c.22_23insA	ENSP00000494225.1:p.Arg8GlnfsTer23
ENST00000642492.1:c.22_23insA	ENSP00000496267.1:p.Arg8GlnfsTer23
ENST00000643738.1:c.22_23insA	ENSP00000493684.1:p.Arg8GlnfsTer23
ENST00000643768.1:n.156_157insA
ENST00000644580.2:c.499_500insA MANE Select	ENSP00000495855.2:p.Arg167GlnfsTer23
ENST00000645572.1:c.499_500insA	ENSP00000494301.1:p.Arg167GlnfsTer23
ENST00000645762.1:n.613_614insA
ENST00000645817.1:c.22_23insA	ENSP00000495731.1:p.Arg8GlnfsTer23
ENST00000647226.1:c.22_23insA	ENSP00000496024.1:p.Arg8GlnfsTer23
ENST00000375129.8:c.499_500insA	ENSP00000364271.4:p.Arg167GlnfsTer23
ENST00000409117.7:c.499_500insA	ENSP00000386647.3:p.Arg167GlnfsTer23
ENST00000437056.5:n.1369_1370insA
ENST00000442710.5:c.341_342insA
ENST00000444615.1:c.141_142insA
NM_001042702.3:c.499_500insA	NP_001036167.1:p.Arg167GlnfsTer23
XM_005246627.1:c.508_509insA	XP_005246684.1:p.Arg170GlnfsTer23
XM_005246628.2:c.604_605insA	XP_005246685.1:p.Arg202GlnfsTer23
XM_005246629.2:c.490_491insA	XP_005246686.1:p.Arg164GlnfsTer23
XM_011511247.1:c.604_605insA	XP_011509549.1:p.Arg202GlnfsTer23
XM_011511248.1:c.568_569insA	XP_011509550.1:p.Arg190GlnfsTer23
XM_011511249.1:c.22_23insA	XP_011509551.1:p.Arg8GlnfsTer23
XM_011511250.1:c.22_23insA	XP_011509552.1:p.Arg8GlnfsTer23
XM_011511251.1:c.22_23insA	XP_011509553.1:p.Arg8GlnfsTer23
XR_922929.1:n.1271_1272insA
NM_001042702.4:c.499_500insA	NP_001036167.1:p.Arg167GlnfsTer23
NM_001353775.1:c.508_509insA	NP_001340704.1:p.Arg170GlnfsTer23
NM_001353776.1:c.604_605insA	NP_001340705.1:p.Arg202GlnfsTer23
NM_001353777.1:c.22_23insA	NP_001340706.1:p.Arg8GlnfsTer23
NM_001353778.1:c.22_23insA	NP_001340707.1:p.Arg8GlnfsTer23
XM_005246629.4:c.490_491insA	XP_005246686.1:p.Arg164GlnfsTer23
XM_011511247.3:c.604_605insA	XP_011509549.1:p.Arg202GlnfsTer23
XM_011511249.3:c.22_23insA	XP_011509551.1:p.Arg8GlnfsTer23
XM_017004221.2:c.604_605insA	XP_016859710.1:p.Arg202GlnfsTer23
XM_017004224.2:c.22_23insA	XP_016859713.1:p.Arg8GlnfsTer23
XM_024452927.1:c.22_23insA	XP_024308695.1:p.Arg8GlnfsTer23
XM_024452928.1:c.22_23insA	XP_024308696.1:p.Arg8GlnfsTer23
XR_001738753.2:n.2311_2312insA
XR_002959300.1:n.2311_2312insA
XR_922929.3:n.794_795insA
NM_001042702.5:c.499_500insA MANE Select	NP_001036167.1:p.Arg167GlnfsTer23
NM_001369912.1:c.499_500insA	NP_001356841.1:p.Arg167GlnfsTer23
NM_001353775.2:c.508_509insA	NP_001340704.1:p.Arg170GlnfsTer23
NM_001353776.2:c.604_605insA	NP_001340705.1:p.Arg202GlnfsTer23
NM_001353778.2:c.22_23insA	NP_001340707.1:p.Arg8GlnfsTer23