Canonical Allele Identifier: CA380370087

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145233A>T (hg19) ; chr11:g.48123681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123681A>T , CM000673.2:g.48123681A>T	GRCh38
NC_000011.9:g.48145233A>T , CM000673.1:g.48145233A>T	GRCh37
NC_000011.8:g.48101809A>T	NCBI36
NG_012209.1:g.148124A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1027A>T	ENSP00000514003.1:p.Asn343Tyr
ENST00000418331.7:c.685A>T MANE Select	ENSP00000400010.2:p.Asn229Tyr
ENST00000418331.6:c.685A>T	ENSP00000400010.2:p.Asn229Tyr
ENST00000440289.6:c.685A>T	ENSP00000409733.2:p.Asn229Tyr
ENST00000527952.1:c.421A>T	ENSP00000435618.1:p.Asn141Tyr
ENST00000613246.4:c.685A>T	ENSP00000477933.1:p.Asn229Tyr
ENST00000615445.4:c.685A>T	ENSP00000479342.1:p.Asn229Tyr
NM_001098503.1:c.685A>T	NP_001091973.1:p.Asn229Tyr
NM_002843.3:c.685A>T	NP_002834.3:p.Asn229Tyr
XM_011520249.1:c.718A>T	XP_011518551.1:p.Asn240Tyr
XR_930883.1:n.1035A>T
XM_017018083.1:c.763A>T	XP_016873572.1:p.Asn255Tyr
XM_017018084.1:c.706A>T	XP_016873573.1:p.Asn236Tyr
XM_017018085.1:c.637A>T	XP_016873574.1:p.Asn213Tyr
XR_930883.2:n.1094A>T
NM_002843.4:c.685A>T MANE Select	NP_002834.3:p.Asn229Tyr
NM_001098503.2:c.685A>T	NP_001091973.1:p.Asn229Tyr