Canonical Allele Identifier: CA13580853
Community Standard Title: NM_030667.3(PTPRO):c.1268-64A>G
Gene: PTPRO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.15508507A>G , CM000674.2:g.15508507A>G GRCh38
NC_000012.11:g.15661441A>G , CM000674.1:g.15661441A>G GRCh37
NC_000012.10:g.15552708A>G NCBI36
NG_031857.1:g.191251A>G

Transcript Alleles

HGVS Amino-acid Change
NM_030667.3:c.1268-64A>G MANE Select NP_109592.1:n.1268-64A>G
ENST00000281171.9:c.1268-64A>G MANE Select ENSP00000281171.4:n.1268-64A>G
NM_002848.3:c.1268-64A>G NP_002839.1:n.1268-64A>G
NM_002848.4:c.1268-64A>G NP_002839.1:n.1268-64A>G
NM_030667.2:c.1268-64A>G NP_109592.1:n.1268-64A>G
ENST00000281171.8:c.1268-64A>G ENSP00000281171.4:n.1268-64A>G
ENST00000348962.6:c.1268-64A>G ENSP00000343434.2:n.1268-64A>G
ENST00000348962.7:c.1268-64A>G ENSP00000343434.2:n.1268-64A>G
ENST00000543886.5:c.1268-64A>G ENSP00000444173.1:n.1268-64A>G
ENST00000543886.6:c.1268-64A>G ENSP00000444173.1:n.1268-64A>G
ENST00000674188.1:c.824-64A>G ENSP00000501325.1:n.824-64A>G
ENST00000674261.1:c.1268-64A>G ENSP00000501538.1:n.1268-64A>G
ENST00000674286.1:c.773-64A>G ENSP00000501361.1:n.773-64A>G
ENST00000674316.1:c.1268-64A>G ENSP00000501352.1:n.1268-64A>G
ENST00000674391.1:c.*730-64A>G ENSP00000501451.1:n.*730-64A>G
XM_011520792.1:c.824-64A>G XP_011519094.1:n.824-64A>G
XM_017019725.2:c.1268-64A>G XP_016875214.1:n.1268-64A>G
XR_931316.1:n.1661-64A>G
XR_931316.3:n.1661-64A>G