Canonical Allele Identifier: CA380370775

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145398C>A (hg19) ; chr11:g.48123846C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123846C>A , CM000673.2:g.48123846C>A	GRCh38
NC_000011.9:g.48145398C>A , CM000673.1:g.48145398C>A	GRCh37
NC_000011.8:g.48101974C>A	NCBI36
NG_012209.1:g.148289C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1192C>A	ENSP00000514003.1:p.Pro398Thr
ENST00000418331.7:c.850C>A MANE Select	ENSP00000400010.2:p.Pro284Thr
ENST00000418331.6:c.850C>A	ENSP00000400010.2:p.Pro284Thr
ENST00000440289.6:c.850C>A	ENSP00000409733.2:p.Pro284Thr
ENST00000613246.4:c.850C>A	ENSP00000477933.1:p.Pro284Thr
ENST00000615445.4:c.850C>A	ENSP00000479342.1:p.Pro284Thr
NM_001098503.1:c.850C>A	NP_001091973.1:p.Pro284Thr
NM_002843.3:c.850C>A	NP_002834.3:p.Pro284Thr
XM_011520249.1:c.883C>A	XP_011518551.1:p.Pro295Thr
XR_930883.1:n.1200C>A
XM_017018083.1:c.928C>A	XP_016873572.1:p.Pro310Thr
XM_017018084.1:c.871C>A	XP_016873573.1:p.Pro291Thr
XM_017018085.1:c.802C>A	XP_016873574.1:p.Pro268Thr
XR_930883.2:n.1259C>A
NM_002843.4:c.850C>A MANE Select	NP_002834.3:p.Pro284Thr
NM_001098503.2:c.850C>A	NP_001091973.1:p.Pro284Thr