Canonical Allele Identifier: CA13706475

Gene: PTPRO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.15578605T>C , CM000674.2:g.15578605T>C	GRCh38
NC_000012.11:g.15731539T>C , CM000674.1:g.15731539T>C	GRCh37
NC_000012.10:g.15622806T>C	NCBI36
NG_031857.1:g.261349T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_030667.3:c.2830-248T>C MANE Select	NP_109592.1:n.2830-248T>C
ENST00000281171.9:c.2830-248T>C MANE Select	ENSP00000281171.4:n.2830-248T>C
NM_002848.3:c.2746-248T>C	NP_002839.1:n.2746-248T>C
NM_002848.4:c.2746-248T>C	NP_002839.1:n.2746-248T>C
NM_030667.2:c.2830-248T>C	NP_109592.1:n.2830-248T>C
NM_030668.2:c.313-248T>C	NP_109593.1:n.313-248T>C
NM_030668.3:c.313-248T>C	NP_109593.1:n.313-248T>C
NM_030669.2:c.397-248T>C	NP_109594.1:n.397-248T>C
NM_030669.3:c.397-248T>C	NP_109594.1:n.397-248T>C
NM_030670.2:c.313-248T>C	NP_109595.1:n.313-248T>C
NM_030670.3:c.313-248T>C	NP_109595.1:n.313-248T>C
NM_030671.2:c.397-248T>C	NP_109596.1:n.397-248T>C
NM_030671.3:c.397-248T>C	NP_109596.1:n.397-248T>C
ENST00000281171.8:c.2830-248T>C	ENSP00000281171.4:n.2830-248T>C
ENST00000348962.6:c.2746-248T>C	ENSP00000343434.2:n.2746-248T>C
ENST00000348962.7:c.2746-248T>C	ENSP00000343434.2:n.2746-248T>C
ENST00000442921.6:c.397-248T>C	ENSP00000404188.2:n.397-248T>C
ENST00000442921.7:c.397-248T>C	ENSP00000404188.2:n.397-248T>C
ENST00000445537.6:c.397-248T>C	ENSP00000393449.2:n.397-248T>C
ENST00000535311.5:c.412-248T>C
ENST00000538907.1:n.363-248T>C
ENST00000542557.5:c.313-248T>C	ENSP00000437571.1:n.313-248T>C
ENST00000544244.5:c.313-248T>C	ENSP00000439234.1:n.313-248T>C
ENST00000544706.2:c.361-248T>C	ENSP00000501413.1:n.361-248T>C
ENST00000674188.1:c.2386-248T>C	ENSP00000501325.1:n.2386-248T>C
ENST00000674220.1:c.444-248T>C	ENSP00000501384.1:n.444-248T>C
ENST00000674261.1:c.2830-248T>C	ENSP00000501538.1:n.2830-248T>C
ENST00000674286.1:c.2335-248T>C	ENSP00000501361.1:n.2335-248T>C
ENST00000674316.1:c.2830-248T>C	ENSP00000501352.1:n.2830-248T>C
ENST00000674352.1:c.650-248T>C
ENST00000674385.1:c.455-248T>C
ENST00000674388.1:c.397-248T>C	ENSP00000501494.1:n.397-248T>C
ENST00000674391.1:c.*2292-248T>C	ENSP00000501451.1:n.*2292-248T>C
ENST00000674434.1:n.1798-248T>C
XM_011520792.1:c.2386-248T>C	XP_011519094.1:n.2386-248T>C
XM_017019725.2:c.*8007T>C	XP_016875214.1:n.*8007T>C
XR_931316.1:n.3223-248T>C
XR_931316.3:n.3223-248T>C
XR_931317.1:n.884-248T>C
XR_931318.1:n.800-248T>C
XR_931318.2:n.795-248T>C