Canonical Allele Identifier: CA474434324

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145217T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123665T>G , CM000673.2:g.48123665T>G	GRCh38
NC_000011.9:g.48145217T>G , CM000673.1:g.48145217T>G	GRCh37
NC_000011.8:g.48101793T>G	NCBI36
NG_012209.1:g.148108T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1011T>G	ENSP00000514003.1:p.Ala337=
ENST00000418331.7:c.669T>G MANE Select	ENSP00000400010.2:p.Ala223=
ENST00000418331.6:c.669T>G	ENSP00000400010.2:p.Ala223=
ENST00000440289.6:c.669T>G	ENSP00000409733.2:p.Ala223=
ENST00000527952.1:c.405T>G	ENSP00000435618.1:p.Ala135=
ENST00000613246.4:c.669T>G	ENSP00000477933.1:p.Ala223=
ENST00000615445.4:c.669T>G	ENSP00000479342.1:p.Ala223=
NM_001098503.1:c.669T>G	NP_001091973.1:p.Ala223=
NM_002843.3:c.669T>G	NP_002834.3:p.Ala223=
XM_011520249.1:c.702T>G	XP_011518551.1:p.Ala234=
XR_930883.1:n.1019T>G
XM_017018083.1:c.747T>G	XP_016873572.1:p.Ala249=
XM_017018084.1:c.690T>G	XP_016873573.1:p.Ala230=
XM_017018085.1:c.621T>G	XP_016873574.1:p.Ala207=
XR_930883.2:n.1078T>G
NM_002843.4:c.669T>G MANE Select	NP_002834.3:p.Ala223=
NM_001098503.2:c.669T>G	NP_001091973.1:p.Ala223=