Canonical Allele Identifier: CA380370693

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1390771374
• gnomAD v2: 11-48145378-C-G
• gnomAD v4: 11-48123826-C-G
• MyVariant Identifiers: chr11:g.48145378C>G (hg19) ; chr11:g.48123826C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123826C>G , CM000673.2:g.48123826C>G	GRCh38
NC_000011.9:g.48145378C>G , CM000673.1:g.48145378C>G	GRCh37
NC_000011.8:g.48101954C>G	NCBI36
NG_012209.1:g.148269C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1172C>G	ENSP00000514003.1:p.Ser391Ter
ENST00000418331.7:c.830C>G MANE Select	ENSP00000400010.2:p.Ser277Ter
ENST00000418331.6:c.830C>G	ENSP00000400010.2:p.Ser277Ter
ENST00000440289.6:c.830C>G	ENSP00000409733.2:p.Ser277Ter
ENST00000613246.4:c.830C>G	ENSP00000477933.1:p.Ser277Ter
ENST00000615445.4:c.830C>G	ENSP00000479342.1:p.Ser277Ter
NM_001098503.1:c.830C>G	NP_001091973.1:p.Ser277Ter
NM_002843.3:c.830C>G	NP_002834.3:p.Ser277Ter
XM_011520249.1:c.863C>G	XP_011518551.1:p.Ser288Ter
XR_930883.1:n.1180C>G
XM_017018083.1:c.908C>G	XP_016873572.1:p.Ser303Ter
XM_017018084.1:c.851C>G	XP_016873573.1:p.Ser284Ter
XM_017018085.1:c.782C>G	XP_016873574.1:p.Ser261Ter
XR_930883.2:n.1239C>G
NM_002843.4:c.830C>G MANE Select	NP_002834.3:p.Ser277Ter
NM_001098503.2:c.830C>G	NP_001091973.1:p.Ser277Ter