Canonical Allele Identifier: CA380369818

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123614-G-C
• MyVariant Identifiers: chr11:g.48145166G>C (hg19) ; chr11:g.48123614G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123614G>C , CM000673.2:g.48123614G>C	GRCh38
NC_000011.9:g.48145166G>C , CM000673.1:g.48145166G>C	GRCh37
NC_000011.8:g.48101742G>C	NCBI36
NG_012209.1:g.148057G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.960G>C	ENSP00000514003.1:p.Glu320Asp
ENST00000418331.7:c.618G>C MANE Select	ENSP00000400010.2:p.Glu206Asp
ENST00000418331.6:c.618G>C	ENSP00000400010.2:p.Glu206Asp
ENST00000440289.6:c.618G>C	ENSP00000409733.2:p.Glu206Asp
ENST00000527952.1:c.354G>C	ENSP00000435618.1:p.Glu118Asp
ENST00000613246.4:c.618G>C	ENSP00000477933.1:p.Glu206Asp
ENST00000615445.4:c.618G>C	ENSP00000479342.1:p.Glu206Asp
NM_001098503.1:c.618G>C	NP_001091973.1:p.Glu206Asp
NM_002843.3:c.618G>C	NP_002834.3:p.Glu206Asp
XM_011520249.1:c.651G>C	XP_011518551.1:p.Glu217Asp
XR_930883.1:n.968G>C
XM_017018083.1:c.696G>C	XP_016873572.1:p.Glu232Asp
XM_017018084.1:c.639G>C	XP_016873573.1:p.Glu213Asp
XM_017018085.1:c.570G>C	XP_016873574.1:p.Glu190Asp
XR_930883.2:n.1027G>C
NM_002843.4:c.618G>C MANE Select	NP_002834.3:p.Glu206Asp
NM_001098503.2:c.618G>C	NP_001091973.1:p.Glu206Asp