Canonical Allele Identifier: CA380370366
Gene: PTPRJ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123754C>G , CM000673.2:g.48123754C>G GRCh38
NC_000011.9:g.48145306C>G , CM000673.1:g.48145306C>G GRCh37
NC_000011.8:g.48101882C>G NCBI36
NG_012209.1:g.148197C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.1100C>G ENSP00000514003.1:p.Ser367Ter
ENST00000418331.7:c.758C>G MANE Select ENSP00000400010.2:p.Ser253Ter
ENST00000418331.6:c.758C>G ENSP00000400010.2:p.Ser253Ter
ENST00000440289.6:c.758C>G ENSP00000409733.2:p.Ser253Ter
ENST00000613246.4:c.758C>G ENSP00000477933.1:p.Ser253Ter
ENST00000615445.4:c.758C>G ENSP00000479342.1:p.Ser253Ter
NM_001098503.1:c.758C>G NP_001091973.1:p.Ser253Ter
NM_002843.3:c.758C>G NP_002834.3:p.Ser253Ter
XM_011520249.1:c.791C>G XP_011518551.1:p.Ser264Ter
XR_930883.1:n.1108C>G
XM_017018083.1:c.836C>G XP_016873572.1:p.Ser279Ter
XM_017018084.1:c.779C>G XP_016873573.1:p.Ser260Ter
XM_017018085.1:c.710C>G XP_016873574.1:p.Ser237Ter
XR_930883.2:n.1167C>G
NM_002843.4:c.758C>G MANE Select NP_002834.3:p.Ser253Ter
NM_001098503.2:c.758C>G NP_001091973.1:p.Ser253Ter