Canonical Allele Identifier: CA2044932888

Gene: PTPRR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.70665152T= , CM000674.2:g.70665152T=	GRCh38
NC_000012.11:g.71058932T= , CM000674.1:g.71058932T=	GRCh37
NC_000012.10:g.69345199T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283228.7:c.1498-2547A= MANE Select	ENSP00000283228.2:n.1498-2547A=
ENST00000283228.6:c.1498-2547A=	ENSP00000283228.2:n.1498-2547A=
ENST00000342084.8:c.1162-2547A=	ENSP00000339605.4:n.1162-2547A=
ENST00000378778.5:c.880-2547A=	ENSP00000368054.1:n.880-2547A=
ENST00000440835.6:c.763-2547A=	ENSP00000391750.2:n.763-2547A=
ENST00000548220.1:n.1046-2547A=
ENST00000549107.5:n.332-2547A=
ENST00000549308.5:c.763-2547A=	ENSP00000446943.1:n.763-2547A=
ENST00000551219.5:c.*126-2547A=	ENSP00000448049.1:n.*126-2547A=
NM_001207015.1:c.1162-2547A=	NP_001193944.1:n.1162-2547A=
NM_001207016.1:c.880-2547A=	NP_001193945.1:n.880-2547A=
NM_002849.3:c.1498-2547A=	NP_002840.2:n.1498-2547A=
NM_130846.2:c.763-2547A=	NP_570897.2:n.763-2547A=
NR_073474.1:n.1248-2547A=
XM_011538615.1:c.1474-2547A=	XP_011536917.1:n.1474-2547A=
XM_011538615.2:c.1474-2547A=	XP_011536917.1:n.1474-2547A=
XR_001748830.1:n.1840-2547A=
XR_001748831.2:n.1281-2547A=
NM_002849.4:c.1498-2547A= MANE Select	NP_002840.2:n.1498-2547A=
NM_001207015.2:c.1162-2547A=	NP_001193944.1:n.1162-2547A=
NM_130846.3:c.763-2547A=	NP_570897.2:n.763-2547A=
NR_073474.2:n.1248-2547A=