Canonical Allele Identifier: CA380370719

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123832-A-T
• MyVariant Identifiers: chr11:g.48145384A>T (hg19) ; chr11:g.48123832A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123832A>T , CM000673.2:g.48123832A>T	GRCh38
NC_000011.9:g.48145384A>T , CM000673.1:g.48145384A>T	GRCh37
NC_000011.8:g.48101960A>T	NCBI36
NG_012209.1:g.148275A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1178A>T	ENSP00000514003.1:p.Lys393Met
ENST00000418331.7:c.836A>T MANE Select	ENSP00000400010.2:p.Lys279Met
ENST00000418331.6:c.836A>T	ENSP00000400010.2:p.Lys279Met
ENST00000440289.6:c.836A>T	ENSP00000409733.2:p.Lys279Met
ENST00000613246.4:c.836A>T	ENSP00000477933.1:p.Lys279Met
ENST00000615445.4:c.836A>T	ENSP00000479342.1:p.Lys279Met
NM_001098503.1:c.836A>T	NP_001091973.1:p.Lys279Met
NM_002843.3:c.836A>T	NP_002834.3:p.Lys279Met
XM_011520249.1:c.869A>T	XP_011518551.1:p.Lys290Met
XR_930883.1:n.1186A>T
XM_017018083.1:c.914A>T	XP_016873572.1:p.Lys305Met
XM_017018084.1:c.857A>T	XP_016873573.1:p.Lys286Met
XM_017018085.1:c.788A>T	XP_016873574.1:p.Lys263Met
XR_930883.2:n.1245A>T
NM_002843.4:c.836A>T MANE Select	NP_002834.3:p.Lys279Met
NM_001098503.2:c.836A>T	NP_001091973.1:p.Lys279Met