Canonical Allele Identifier: CA380370737

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145387C>G (hg19) ; chr11:g.48123835C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123835C>G , CM000673.2:g.48123835C>G	GRCh38
NC_000011.9:g.48145387C>G , CM000673.1:g.48145387C>G	GRCh37
NC_000011.8:g.48101963C>G	NCBI36
NG_012209.1:g.148278C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1181C>G	ENSP00000514003.1:p.Thr394Arg
ENST00000418331.7:c.839C>G MANE Select	ENSP00000400010.2:p.Thr280Arg
ENST00000418331.6:c.839C>G	ENSP00000400010.2:p.Thr280Arg
ENST00000440289.6:c.839C>G	ENSP00000409733.2:p.Thr280Arg
ENST00000613246.4:c.839C>G	ENSP00000477933.1:p.Thr280Arg
ENST00000615445.4:c.839C>G	ENSP00000479342.1:p.Thr280Arg
NM_001098503.1:c.839C>G	NP_001091973.1:p.Thr280Arg
NM_002843.3:c.839C>G	NP_002834.3:p.Thr280Arg
XM_011520249.1:c.872C>G	XP_011518551.1:p.Thr291Arg
XR_930883.1:n.1189C>G
XM_017018083.1:c.917C>G	XP_016873572.1:p.Thr306Arg
XM_017018084.1:c.860C>G	XP_016873573.1:p.Thr287Arg
XM_017018085.1:c.791C>G	XP_016873574.1:p.Thr264Arg
XR_930883.2:n.1248C>G
NM_002843.4:c.839C>G MANE Select	NP_002834.3:p.Thr280Arg
NM_001098503.2:c.839C>G	NP_001091973.1:p.Thr280Arg