Canonical Allele Identifier: CA349397446

Gene: PJVK

Linked Data

• MyVariant Identifiers: chr2:g.179318302T>C (hg19) ; chr2:g.178453575T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178453575T>C , CM000664.2:g.178453575T>C	GRCh38
NC_000002.11:g.179318302T>C , CM000664.1:g.179318302T>C	GRCh37
NC_000002.10:g.179026548T>C	NCBI36
NG_009053.1:g.2657A>G
NG_012186.1:g.7140T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000642192.1:c.-312T>C	ENSP00000494225.1:n.-312T>C
ENST00000642492.1:c.-413T>C	ENSP00000496267.1:n.-413T>C
ENST00000643738.1:c.-312T>C	ENSP00000493684.1:n.-312T>C
ENST00000644554.1:c.-312T>C	ENSP00000495037.1:n.-312T>C
ENST00000644580.2:c.166T>C MANE Select	ENSP00000495855.2:p.Phe56Leu
ENST00000645572.1:c.166T>C	ENSP00000494301.1:p.Phe56Leu
ENST00000645762.1:n.280T>C
ENST00000645817.1:c.-312T>C	ENSP00000495731.1:n.-312T>C
ENST00000647226.1:c.-312T>C	ENSP00000496024.1:n.-312T>C
ENST00000375129.8:c.166T>C	ENSP00000364271.4:p.Phe56Leu
ENST00000409117.7:c.166T>C	ENSP00000386647.3:p.Phe56Leu
ENST00000437056.5:n.325T>C
ENST00000442710.5:c.8T>C
NM_001042702.3:c.166T>C	NP_001036167.1:p.Phe56Leu
XM_005246627.1:c.175T>C	XP_005246684.1:p.Phe59Leu
XM_005246628.2:c.271T>C	XP_005246685.1:p.Phe91Leu
XM_005246629.2:c.157T>C	XP_005246686.1:p.Phe53Leu
XM_011511247.1:c.271T>C	XP_011509549.1:p.Phe91Leu
XM_011511248.1:c.235T>C	XP_011509550.1:p.Phe79Leu
XM_011511249.1:c.-266-757T>C	XP_011509551.1:n.-266-757T>C
XM_011511250.1:c.-312T>C	XP_011509552.1:n.-312T>C
XM_011511251.1:c.-266-757T>C	XP_011509553.1:n.-266-757T>C
XR_922929.1:n.938T>C
NM_001042702.4:c.166T>C	NP_001036167.1:p.Phe56Leu
NM_001353775.1:c.175T>C	NP_001340704.1:p.Phe59Leu
NM_001353776.1:c.271T>C	NP_001340705.1:p.Phe91Leu
NM_001353777.1:c.-312T>C	NP_001340706.1:n.-312T>C
NM_001353778.1:c.-312T>C	NP_001340707.1:n.-312T>C
XM_005246629.4:c.157T>C	XP_005246686.1:p.Phe53Leu
XM_011511247.3:c.271T>C	XP_011509549.1:p.Phe91Leu
XM_011511249.3:c.-266-757T>C	XP_011509551.1:n.-266-757T>C
XM_017004221.2:c.271T>C	XP_016859710.1:p.Phe91Leu
XM_017004224.2:c.-1023T>C	XP_016859713.1:n.-1023T>C
XM_024452927.1:c.-413T>C	XP_024308695.1:n.-413T>C
XM_024452928.1:c.-312T>C	XP_024308696.1:n.-312T>C
XR_001738753.2:n.1978T>C
XR_002959300.1:n.1978T>C
XR_922929.3:n.461T>C
NM_001042702.5:c.166T>C MANE Select	NP_001036167.1:p.Phe56Leu
NM_001369912.1:c.166T>C	NP_001356841.1:p.Phe56Leu
NM_001353775.2:c.175T>C	NP_001340704.1:p.Phe59Leu
NM_001353776.2:c.271T>C	NP_001340705.1:p.Phe91Leu
NM_001353778.2:c.-312T>C	NP_001340707.1:n.-312T>C