Canonical Allele Identifier: CA2044941483

Gene: PTPRR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.70679733A= , CM000674.2:g.70679733A=	GRCh38
NC_000012.11:g.71073513A= , CM000674.1:g.71073513A=	GRCh37
NC_000012.10:g.69359780A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002849.4:c.1497+4394T= MANE Select	NP_002840.2:n.1497+4394T=
ENST00000283228.7:c.1497+4394T= MANE Select	ENSP00000283228.2:n.1497+4394T=
NM_001207015.1:c.1161+4394T=	NP_001193944.1:n.1161+4394T=
NM_001207015.2:c.1161+4394T=	NP_001193944.1:n.1161+4394T=
NM_001207016.1:c.879+4394T=	NP_001193945.1:n.879+4394T=
NM_002849.3:c.1497+4394T=	NP_002840.2:n.1497+4394T=
NM_130846.2:c.762+4394T=	NP_570897.2:n.762+4394T=
NM_130846.3:c.762+4394T=	NP_570897.2:n.762+4394T=
NR_073474.1:n.990+4394T=
NR_073474.2:n.990+4394T=
ENST00000283228.6:c.1497+4394T=	ENSP00000283228.2:n.1497+4394T=
ENST00000342084.8:c.1161+4394T=	ENSP00000339605.4:n.1161+4394T=
ENST00000378778.5:c.879+4394T=	ENSP00000368054.1:n.879+4394T=
ENST00000440835.6:c.762+4394T=	ENSP00000391750.2:n.762+4394T=
ENST00000548220.1:n.1045+4394T=
ENST00000549107.5:n.331+4394T=
ENST00000549308.5:c.762+4394T=	ENSP00000446943.1:n.762+4394T=
ENST00000551219.5:c.294+4394T=	ENSP00000448049.1:n.294+4394T=
XM_011538615.1:c.1473+4394T=	XP_011536917.1:n.1473+4394T=
XM_011538615.2:c.1473+4394T=	XP_011536917.1:n.1473+4394T=
XM_011538616.1:c.1497+4394T=	XP_011536918.1:n.1497+4394T=
XR_001748830.1:n.1839+4394T=
XR_001748831.2:n.1280+4394T=