Canonical Allele Identifier: CA380370018

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145216C>A (hg19) ; chr11:g.48123664C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123664C>A , CM000673.2:g.48123664C>A	GRCh38
NC_000011.9:g.48145216C>A , CM000673.1:g.48145216C>A	GRCh37
NC_000011.8:g.48101792C>A	NCBI36
NG_012209.1:g.148107C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1010C>A	ENSP00000514003.1:p.Ala337Asp
ENST00000418331.7:c.668C>A MANE Select	ENSP00000400010.2:p.Ala223Asp
ENST00000418331.6:c.668C>A	ENSP00000400010.2:p.Ala223Asp
ENST00000440289.6:c.668C>A	ENSP00000409733.2:p.Ala223Asp
ENST00000527952.1:c.404C>A	ENSP00000435618.1:p.Ala135Asp
ENST00000613246.4:c.668C>A	ENSP00000477933.1:p.Ala223Asp
ENST00000615445.4:c.668C>A	ENSP00000479342.1:p.Ala223Asp
NM_001098503.1:c.668C>A	NP_001091973.1:p.Ala223Asp
NM_002843.3:c.668C>A	NP_002834.3:p.Ala223Asp
XM_011520249.1:c.701C>A	XP_011518551.1:p.Ala234Asp
XR_930883.1:n.1018C>A
XM_017018083.1:c.746C>A	XP_016873572.1:p.Ala249Asp
XM_017018084.1:c.689C>A	XP_016873573.1:p.Ala230Asp
XM_017018085.1:c.620C>A	XP_016873574.1:p.Ala207Asp
XR_930883.2:n.1077C>A
NM_002843.4:c.668C>A MANE Select	NP_002834.3:p.Ala223Asp
NM_001098503.2:c.668C>A	NP_001091973.1:p.Ala223Asp