Canonical Allele Identifier: CA474434293

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145178T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123626T>G , CM000673.2:g.48123626T>G	GRCh38
NC_000011.9:g.48145178T>G , CM000673.1:g.48145178T>G	GRCh37
NC_000011.8:g.48101754T>G	NCBI36
NG_012209.1:g.148069T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.972T>G	ENSP00000514003.1:p.Val324=
ENST00000418331.7:c.630T>G MANE Select	ENSP00000400010.2:p.Val210=
ENST00000418331.6:c.630T>G	ENSP00000400010.2:p.Val210=
ENST00000440289.6:c.630T>G	ENSP00000409733.2:p.Val210=
ENST00000527952.1:c.366T>G	ENSP00000435618.1:p.Val122=
ENST00000613246.4:c.630T>G	ENSP00000477933.1:p.Val210=
ENST00000615445.4:c.630T>G	ENSP00000479342.1:p.Val210=
NM_001098503.1:c.630T>G	NP_001091973.1:p.Val210=
NM_002843.3:c.630T>G	NP_002834.3:p.Val210=
XM_011520249.1:c.663T>G	XP_011518551.1:p.Val221=
XR_930883.1:n.980T>G
XM_017018083.1:c.708T>G	XP_016873572.1:p.Val236=
XM_017018084.1:c.651T>G	XP_016873573.1:p.Val217=
XM_017018085.1:c.582T>G	XP_016873574.1:p.Val194=
XR_930883.2:n.1039T>G
NM_002843.4:c.630T>G MANE Select	NP_002834.3:p.Val210=
NM_001098503.2:c.630T>G	NP_001091973.1:p.Val210=