Canonical Allele Identifier: CA474434318

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145208G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123656G>T , CM000673.2:g.48123656G>T	GRCh38
NC_000011.9:g.48145208G>T , CM000673.1:g.48145208G>T	GRCh37
NC_000011.8:g.48101784G>T	NCBI36
NG_012209.1:g.148099G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1002G>T	ENSP00000514003.1:p.Val334=
ENST00000418331.7:c.660G>T MANE Select	ENSP00000400010.2:p.Val220=
ENST00000418331.6:c.660G>T	ENSP00000400010.2:p.Val220=
ENST00000440289.6:c.660G>T	ENSP00000409733.2:p.Val220=
ENST00000527952.1:c.396G>T	ENSP00000435618.1:p.Val132=
ENST00000613246.4:c.660G>T	ENSP00000477933.1:p.Val220=
ENST00000615445.4:c.660G>T	ENSP00000479342.1:p.Val220=
NM_001098503.1:c.660G>T	NP_001091973.1:p.Val220=
NM_002843.3:c.660G>T	NP_002834.3:p.Val220=
XM_011520249.1:c.693G>T	XP_011518551.1:p.Val231=
XR_930883.1:n.1010G>T
XM_017018083.1:c.738G>T	XP_016873572.1:p.Val246=
XM_017018084.1:c.681G>T	XP_016873573.1:p.Val227=
XM_017018085.1:c.612G>T	XP_016873574.1:p.Val204=
XR_930883.2:n.1069G>T
NM_002843.4:c.660G>T MANE Select	NP_002834.3:p.Val220=
NM_001098503.2:c.660G>T	NP_001091973.1:p.Val220=