Canonical Allele Identifier: CA380370701

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123829-A-C
• MyVariant Identifiers: chr11:g.48145381A>C (hg19) ; chr11:g.48123829A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123829A>C , CM000673.2:g.48123829A>C	GRCh38
NC_000011.9:g.48145381A>C , CM000673.1:g.48145381A>C	GRCh37
NC_000011.8:g.48101957A>C	NCBI36
NG_012209.1:g.148272A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1175A>C	ENSP00000514003.1:p.Asn392Thr
ENST00000418331.7:c.833A>C MANE Select	ENSP00000400010.2:p.Asn278Thr
ENST00000418331.6:c.833A>C	ENSP00000400010.2:p.Asn278Thr
ENST00000440289.6:c.833A>C	ENSP00000409733.2:p.Asn278Thr
ENST00000613246.4:c.833A>C	ENSP00000477933.1:p.Asn278Thr
ENST00000615445.4:c.833A>C	ENSP00000479342.1:p.Asn278Thr
NM_001098503.1:c.833A>C	NP_001091973.1:p.Asn278Thr
NM_002843.3:c.833A>C	NP_002834.3:p.Asn278Thr
XM_011520249.1:c.866A>C	XP_011518551.1:p.Asn289Thr
XR_930883.1:n.1183A>C
XM_017018083.1:c.911A>C	XP_016873572.1:p.Asn304Thr
XM_017018084.1:c.854A>C	XP_016873573.1:p.Asn285Thr
XM_017018085.1:c.785A>C	XP_016873574.1:p.Asn262Thr
XR_930883.2:n.1242A>C
NM_002843.4:c.833A>C MANE Select	NP_002834.3:p.Asn278Thr
NM_001098503.2:c.833A>C	NP_001091973.1:p.Asn278Thr