Canonical Allele Identifier: CA474434341

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145244C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123692C>G , CM000673.2:g.48123692C>G	GRCh38
NC_000011.9:g.48145244C>G , CM000673.1:g.48145244C>G	GRCh37
NC_000011.8:g.48101820C>G	NCBI36
NG_012209.1:g.148135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1038C>G	ENSP00000514003.1:p.Gly346=
ENST00000418331.7:c.696C>G MANE Select	ENSP00000400010.2:p.Gly232=
ENST00000418331.6:c.696C>G	ENSP00000400010.2:p.Gly232=
ENST00000440289.6:c.696C>G	ENSP00000409733.2:p.Gly232=
ENST00000527952.1:c.432C>G	ENSP00000435618.1:p.Gly144=
ENST00000613246.4:c.696C>G	ENSP00000477933.1:p.Gly232=
ENST00000615445.4:c.696C>G	ENSP00000479342.1:p.Gly232=
NM_001098503.1:c.696C>G	NP_001091973.1:p.Gly232=
NM_002843.3:c.696C>G	NP_002834.3:p.Gly232=
XM_011520249.1:c.729C>G	XP_011518551.1:p.Gly243=
XR_930883.1:n.1046C>G
XM_017018083.1:c.774C>G	XP_016873572.1:p.Gly258=
XM_017018084.1:c.717C>G	XP_016873573.1:p.Gly239=
XM_017018085.1:c.648C>G	XP_016873574.1:p.Gly216=
XR_930883.2:n.1105C>G
NM_002843.4:c.696C>G MANE Select	NP_002834.3:p.Gly232=
NM_001098503.2:c.696C>G	NP_001091973.1:p.Gly232=