Canonical Allele Identifier: CA1969701932

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1856773411

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123935A>C , CM000673.2:g.48123935A>C	GRCh38
NC_000011.9:g.48145487A>C , CM000673.1:g.48145487A>C	GRCh37
NC_000011.8:g.48102063A>C	NCBI36
NG_012209.1:g.148378A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1216+65A>C	ENSP00000514003.1:n.1216+65A>C
ENST00000418331.7:c.874+65A>C MANE Select	ENSP00000400010.2:n.874+65A>C
ENST00000418331.6:c.874+65A>C	ENSP00000400010.2:n.874+65A>C
ENST00000440289.6:c.874+65A>C	ENSP00000409733.2:n.874+65A>C
ENST00000613246.4:c.874+65A>C	ENSP00000477933.1:n.874+65A>C
ENST00000615445.4:c.874+65A>C	ENSP00000479342.1:n.874+65A>C
NM_001098503.1:c.874+65A>C	NP_001091973.1:n.874+65A>C
NM_002843.3:c.874+65A>C	NP_002834.3:n.874+65A>C
XM_011520249.1:c.907+65A>C	XP_011518551.1:n.907+65A>C
XR_930883.1:n.1224+65A>C
XM_017018083.1:c.952+65A>C	XP_016873572.1:n.952+65A>C
XM_017018084.1:c.895+65A>C	XP_016873573.1:n.895+65A>C
XM_017018085.1:c.826+65A>C	XP_016873574.1:n.826+65A>C
XR_930883.2:n.1283+65A>C
NM_002843.4:c.874+65A>C MANE Select	NP_002834.3:n.874+65A>C
NM_001098503.2:c.874+65A>C	NP_001091973.1:n.874+65A>C