Canonical Allele Identifier: CA380369847

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145171T>C (hg19) ; chr11:g.48123619T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123619T>C , CM000673.2:g.48123619T>C	GRCh38
NC_000011.9:g.48145171T>C , CM000673.1:g.48145171T>C	GRCh37
NC_000011.8:g.48101747T>C	NCBI36
NG_012209.1:g.148062T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.965T>C	ENSP00000514003.1:p.Ile322Thr
ENST00000418331.7:c.623T>C MANE Select	ENSP00000400010.2:p.Ile208Thr
ENST00000418331.6:c.623T>C	ENSP00000400010.2:p.Ile208Thr
ENST00000440289.6:c.623T>C	ENSP00000409733.2:p.Ile208Thr
ENST00000527952.1:c.359T>C	ENSP00000435618.1:p.Ile120Thr
ENST00000613246.4:c.623T>C	ENSP00000477933.1:p.Ile208Thr
ENST00000615445.4:c.623T>C	ENSP00000479342.1:p.Ile208Thr
NM_001098503.1:c.623T>C	NP_001091973.1:p.Ile208Thr
NM_002843.3:c.623T>C	NP_002834.3:p.Ile208Thr
XM_011520249.1:c.656T>C	XP_011518551.1:p.Ile219Thr
XR_930883.1:n.973T>C
XM_017018083.1:c.701T>C	XP_016873572.1:p.Ile234Thr
XM_017018084.1:c.644T>C	XP_016873573.1:p.Ile215Thr
XM_017018085.1:c.575T>C	XP_016873574.1:p.Ile192Thr
XR_930883.2:n.1032T>C
NM_002843.4:c.623T>C MANE Select	NP_002834.3:p.Ile208Thr
NM_001098503.2:c.623T>C	NP_001091973.1:p.Ile208Thr