Canonical Allele Identifier: CA380370827

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145412A>C (hg19) ; chr11:g.48123860A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123860A>C , CM000673.2:g.48123860A>C	GRCh38
NC_000011.9:g.48145412A>C , CM000673.1:g.48145412A>C	GRCh37
NC_000011.8:g.48101988A>C	NCBI36
NG_012209.1:g.148303A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1206A>C	ENSP00000514003.1:p.Glu402Asp
ENST00000418331.7:c.864A>C MANE Select	ENSP00000400010.2:p.Glu288Asp
ENST00000418331.6:c.864A>C	ENSP00000400010.2:p.Glu288Asp
ENST00000440289.6:c.864A>C	ENSP00000409733.2:p.Glu288Asp
ENST00000613246.4:c.864A>C	ENSP00000477933.1:p.Glu288Asp
ENST00000615445.4:c.864A>C	ENSP00000479342.1:p.Glu288Asp
NM_001098503.1:c.864A>C	NP_001091973.1:p.Glu288Asp
NM_002843.3:c.864A>C	NP_002834.3:p.Glu288Asp
XM_011520249.1:c.897A>C	XP_011518551.1:p.Glu299Asp
XR_930883.1:n.1214A>C
XM_017018083.1:c.942A>C	XP_016873572.1:p.Glu314Asp
XM_017018084.1:c.885A>C	XP_016873573.1:p.Glu295Asp
XM_017018085.1:c.816A>C	XP_016873574.1:p.Glu272Asp
XR_930883.2:n.1273A>C
NM_002843.4:c.864A>C MANE Select	NP_002834.3:p.Glu288Asp
NM_001098503.2:c.864A>C	NP_001091973.1:p.Glu288Asp