Canonical Allele Identifier: CA474434497

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145388A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123836A>C , CM000673.2:g.48123836A>C	GRCh38
NC_000011.9:g.48145388A>C , CM000673.1:g.48145388A>C	GRCh37
NC_000011.8:g.48101964A>C	NCBI36
NG_012209.1:g.148279A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1182A>C	ENSP00000514003.1:p.Thr394=
ENST00000418331.7:c.840A>C MANE Select	ENSP00000400010.2:p.Thr280=
ENST00000418331.6:c.840A>C	ENSP00000400010.2:p.Thr280=
ENST00000440289.6:c.840A>C	ENSP00000409733.2:p.Thr280=
ENST00000613246.4:c.840A>C	ENSP00000477933.1:p.Thr280=
ENST00000615445.4:c.840A>C	ENSP00000479342.1:p.Thr280=
NM_001098503.1:c.840A>C	NP_001091973.1:p.Thr280=
NM_002843.3:c.840A>C	NP_002834.3:p.Thr280=
XM_011520249.1:c.873A>C	XP_011518551.1:p.Thr291=
XR_930883.1:n.1190A>C
XM_017018083.1:c.918A>C	XP_016873572.1:p.Thr306=
XM_017018084.1:c.861A>C	XP_016873573.1:p.Thr287=
XM_017018085.1:c.792A>C	XP_016873574.1:p.Thr264=
XR_930883.2:n.1249A>C
NM_002843.4:c.840A>C MANE Select	NP_002834.3:p.Thr280=
NM_001098503.2:c.840A>C	NP_001091973.1:p.Thr280=