Canonical Allele Identifier: CA474434334

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145235T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123683T>C , CM000673.2:g.48123683T>C	GRCh38
NC_000011.9:g.48145235T>C , CM000673.1:g.48145235T>C	GRCh37
NC_000011.8:g.48101811T>C	NCBI36
NG_012209.1:g.148126T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1029T>C	ENSP00000514003.1:p.Asn343=
ENST00000418331.7:c.687T>C MANE Select	ENSP00000400010.2:p.Asn229=
ENST00000418331.6:c.687T>C	ENSP00000400010.2:p.Asn229=
ENST00000440289.6:c.687T>C	ENSP00000409733.2:p.Asn229=
ENST00000527952.1:c.423T>C	ENSP00000435618.1:p.Asn141=
ENST00000613246.4:c.687T>C	ENSP00000477933.1:p.Asn229=
ENST00000615445.4:c.687T>C	ENSP00000479342.1:p.Asn229=
NM_001098503.1:c.687T>C	NP_001091973.1:p.Asn229=
NM_002843.3:c.687T>C	NP_002834.3:p.Asn229=
XM_011520249.1:c.720T>C	XP_011518551.1:p.Asn240=
XR_930883.1:n.1037T>C
XM_017018083.1:c.765T>C	XP_016873572.1:p.Asn255=
XM_017018084.1:c.708T>C	XP_016873573.1:p.Asn236=
XM_017018085.1:c.639T>C	XP_016873574.1:p.Asn213=
XR_930883.2:n.1096T>C
NM_002843.4:c.687T>C MANE Select	NP_002834.3:p.Asn229=
NM_001098503.2:c.687T>C	NP_001091973.1:p.Asn229=