Canonical Allele Identifier: CA380369813

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145165A>C (hg19) ; chr11:g.48123613A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123613A>C , CM000673.2:g.48123613A>C	GRCh38
NC_000011.9:g.48145165A>C , CM000673.1:g.48145165A>C	GRCh37
NC_000011.8:g.48101741A>C	NCBI36
NG_012209.1:g.148056A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.959A>C	ENSP00000514003.1:p.Glu320Ala
ENST00000418331.7:c.617A>C MANE Select	ENSP00000400010.2:p.Glu206Ala
ENST00000418331.6:c.617A>C	ENSP00000400010.2:p.Glu206Ala
ENST00000440289.6:c.617A>C	ENSP00000409733.2:p.Glu206Ala
ENST00000527952.1:c.353A>C	ENSP00000435618.1:p.Glu118Ala
ENST00000613246.4:c.617A>C	ENSP00000477933.1:p.Glu206Ala
ENST00000615445.4:c.617A>C	ENSP00000479342.1:p.Glu206Ala
NM_001098503.1:c.617A>C	NP_001091973.1:p.Glu206Ala
NM_002843.3:c.617A>C	NP_002834.3:p.Glu206Ala
XM_011520249.1:c.650A>C	XP_011518551.1:p.Glu217Ala
XR_930883.1:n.967A>C
XM_017018083.1:c.695A>C	XP_016873572.1:p.Glu232Ala
XM_017018084.1:c.638A>C	XP_016873573.1:p.Glu213Ala
XM_017018085.1:c.569A>C	XP_016873574.1:p.Glu190Ala
XR_930883.2:n.1026A>C
NM_002843.4:c.617A>C MANE Select	NP_002834.3:p.Glu206Ala
NM_001098503.2:c.617A>C	NP_001091973.1:p.Glu206Ala