Canonical Allele Identifier: CA474434343

Gene: PTPRJ

Linked Data

• dbSNP Id: rs2270992
• MyVariant Identifiers: chr11:g.48145247T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123695T>A , CM000673.2:g.48123695T>A	GRCh38
NC_000011.9:g.48145247T>A , CM000673.1:g.48145247T>A	GRCh37
NC_000011.8:g.48101823T>A	NCBI36
NG_012209.1:g.148138T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1041T>A	ENSP00000514003.1:p.Thr347=
ENST00000418331.7:c.699T>A MANE Select	ENSP00000400010.2:p.Thr233=
ENST00000418331.6:c.699T>A	ENSP00000400010.2:p.Thr233=
ENST00000440289.6:c.699T>A	ENSP00000409733.2:p.Thr233=
ENST00000527952.1:c.435T>A	ENSP00000435618.1:p.Thr145=
ENST00000613246.4:c.699T>A	ENSP00000477933.1:p.Thr233=
ENST00000615445.4:c.699T>A	ENSP00000479342.1:p.Thr233=
NM_001098503.1:c.699T>A	NP_001091973.1:p.Thr233=
NM_002843.3:c.699T>A	NP_002834.3:p.Thr233=
XM_011520249.1:c.732T>A	XP_011518551.1:p.Thr244=
XR_930883.1:n.1049T>A
XM_017018083.1:c.777T>A	XP_016873572.1:p.Thr259=
XM_017018084.1:c.720T>A	XP_016873573.1:p.Thr240=
XM_017018085.1:c.651T>A	XP_016873574.1:p.Thr217=
XR_930883.2:n.1108T>A
NM_002843.4:c.699T>A MANE Select	NP_002834.3:p.Thr233=
NM_001098503.2:c.699T>A	NP_001091973.1:p.Thr233=