Canonical Allele Identifier: CA380370136

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145245A>G (hg19) ; chr11:g.48123693A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123693A>G , CM000673.2:g.48123693A>G	GRCh38
NC_000011.9:g.48145245A>G , CM000673.1:g.48145245A>G	GRCh37
NC_000011.8:g.48101821A>G	NCBI36
NG_012209.1:g.148136A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1039A>G	ENSP00000514003.1:p.Thr347Ala
ENST00000418331.7:c.697A>G MANE Select	ENSP00000400010.2:p.Thr233Ala
ENST00000418331.6:c.697A>G	ENSP00000400010.2:p.Thr233Ala
ENST00000440289.6:c.697A>G	ENSP00000409733.2:p.Thr233Ala
ENST00000527952.1:c.433A>G	ENSP00000435618.1:p.Thr145Ala
ENST00000613246.4:c.697A>G	ENSP00000477933.1:p.Thr233Ala
ENST00000615445.4:c.697A>G	ENSP00000479342.1:p.Thr233Ala
NM_001098503.1:c.697A>G	NP_001091973.1:p.Thr233Ala
NM_002843.3:c.697A>G	NP_002834.3:p.Thr233Ala
XM_011520249.1:c.730A>G	XP_011518551.1:p.Thr244Ala
XR_930883.1:n.1047A>G
XM_017018083.1:c.775A>G	XP_016873572.1:p.Thr259Ala
XM_017018084.1:c.718A>G	XP_016873573.1:p.Thr240Ala
XM_017018085.1:c.649A>G	XP_016873574.1:p.Thr217Ala
XR_930883.2:n.1106A>G
NM_002843.4:c.697A>G MANE Select	NP_002834.3:p.Thr233Ala
NM_001098503.2:c.697A>G	NP_001091973.1:p.Thr233Ala