Canonical Allele Identifier: CA233323368

Gene: PTPRO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.15516485_15516488del , CM000674.2:g.15516485_15516488del	GRCh38
NC_000012.11:g.15669419_15669422del , CM000674.1:g.15669419_15669422del	GRCh37
NC_000012.10:g.15560686_15560689del	NCBI36
NG_031857.1:g.199229_199232del

Transcript Alleles

HGVS	Amino-acid Change
NM_030667.3:c.1586-278_1586-275del MANE Select	NP_109592.1:n.1586-278_1586-275del
ENST00000281171.9:c.1586-278_1586-275del MANE Select	ENSP00000281171.4:n.1586-278_1586-275del
NM_002848.3:c.1586-278_1586-275del	NP_002839.1:n.1586-278_1586-275del
NM_002848.4:c.1586-278_1586-275del	NP_002839.1:n.1586-278_1586-275del
NM_030667.2:c.1586-278_1586-275del	NP_109592.1:n.1586-278_1586-275del
ENST00000281171.8:c.1586-278_1586-275del	ENSP00000281171.4:n.1586-278_1586-275del
ENST00000348962.6:c.1586-278_1586-275del	ENSP00000343434.2:n.1586-278_1586-275del
ENST00000348962.7:c.1586-278_1586-275del	ENSP00000343434.2:n.1586-278_1586-275del
ENST00000543886.5:c.1586-278_1586-275del	ENSP00000444173.1:n.1586-278_1586-275del
ENST00000543886.6:c.1586-278_1586-275del	ENSP00000444173.1:n.1586-278_1586-275del
ENST00000674188.1:c.1142-278_1142-275del	ENSP00000501325.1:n.1142-278_1142-275del
ENST00000674261.1:c.1586-278_1586-275del	ENSP00000501538.1:n.1586-278_1586-275del
ENST00000674286.1:c.1091-278_1091-275del	ENSP00000501361.1:n.1091-278_1091-275del
ENST00000674316.1:c.1586-278_1586-275del	ENSP00000501352.1:n.1586-278_1586-275del
ENST00000674391.1:c.*1048-278_*1048-275del	ENSP00000501451.1:n.*1048-278_*1048-275del
XM_011520792.1:c.1142-278_1142-275del	XP_011519094.1:n.1142-278_1142-275del
XM_017019725.2:c.1586-278_1586-275del	XP_016875214.1:n.1586-278_1586-275del
XR_931316.1:n.1979-278_1979-275del
XR_931316.3:n.1979-278_1979-275del