Canonical Allele Identifier: CA349400267

Gene: PJVK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178458520T>C , CM000664.2:g.178458520T>C	GRCh38
NC_000002.11:g.179323247T>C , CM000664.1:g.179323247T>C	GRCh37
NC_000002.10:g.179031493T>C	NCBI36
NG_012186.1:g.12085T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001042702.5:c.560T>C MANE Select	NP_001036167.1:p.Met187Thr
ENST00000644580.2:c.560T>C MANE Select	ENSP00000495855.2:p.Met187Thr
NM_001042702.3:c.560T>C	NP_001036167.1:p.Met187Thr
NM_001042702.4:c.560T>C	NP_001036167.1:p.Met187Thr
NM_001353775.1:c.569T>C	NP_001340704.1:p.Met190Thr
NM_001353775.2:c.569T>C	NP_001340704.1:p.Met190Thr
NM_001353776.1:c.665T>C	NP_001340705.1:p.Met222Thr
NM_001353776.2:c.665T>C	NP_001340705.1:p.Met222Thr
NM_001353777.1:c.83T>C	NP_001340706.1:p.Met28Thr
NM_001353778.1:c.83T>C	NP_001340707.1:p.Met28Thr
NM_001353778.2:c.83T>C	NP_001340707.1:p.Met28Thr
NM_001369912.1:c.560T>C	NP_001356841.1:p.Met187Thr
ENST00000375129.8:c.560T>C	ENSP00000364271.4:p.Met187Thr
ENST00000409117.7:c.560T>C	ENSP00000386647.3:p.Met187Thr
ENST00000437056.5:n.1430T>C
ENST00000442710.5:c.392-1828T>C
ENST00000444615.1:c.202T>C
ENST00000642192.1:c.83T>C	ENSP00000494225.1:p.Met28Thr
ENST00000642492.1:c.83T>C	ENSP00000496267.1:p.Met28Thr
ENST00000643738.1:c.83T>C	ENSP00000493684.1:p.Met28Thr
ENST00000643768.1:n.217T>C
ENST00000645572.1:c.560T>C	ENSP00000494301.1:p.Met187Thr
ENST00000645817.1:c.83T>C	ENSP00000495731.1:p.Met28Thr
ENST00000647226.1:c.83T>C	ENSP00000496024.1:p.Met28Thr
XM_005246627.1:c.569T>C	XP_005246684.1:p.Met190Thr
XM_005246628.2:c.665T>C	XP_005246685.1:p.Met222Thr
XM_005246629.2:c.551T>C	XP_005246686.1:p.Met184Thr
XM_005246629.4:c.551T>C	XP_005246686.1:p.Met184Thr
XM_011511247.1:c.665T>C	XP_011509549.1:p.Met222Thr
XM_011511247.3:c.665T>C	XP_011509549.1:p.Met222Thr
XM_011511248.1:c.629T>C	XP_011509550.1:p.Met210Thr
XM_011511249.1:c.83T>C	XP_011509551.1:p.Met28Thr
XM_011511249.3:c.83T>C	XP_011509551.1:p.Met28Thr
XM_011511250.1:c.83T>C	XP_011509552.1:p.Met28Thr
XM_011511251.1:c.83T>C	XP_011509553.1:p.Met28Thr
XM_017004221.2:c.665T>C	XP_016859710.1:p.Met222Thr
XM_017004224.2:c.83T>C	XP_016859713.1:p.Met28Thr
XM_024452927.1:c.83T>C	XP_024308695.1:p.Met28Thr
XM_024452928.1:c.83T>C	XP_024308696.1:p.Met28Thr
XR_001738753.2:n.2372T>C
XR_002959300.1:n.2372T>C
XR_922929.1:n.1332T>C
XR_922929.3:n.855T>C