Canonical Allele Identifier: CA13670116

Gene: PTPRR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.70741742G>T , CM000674.2:g.70741742G>T	GRCh38
NC_000012.11:g.71135522G>T , CM000674.1:g.71135522G>T	GRCh37
NC_000012.10:g.69421789G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283228.7:c.1007+4076C>A MANE Select	ENSP00000283228.2:n.1007+4076C>A
ENST00000283228.6:c.1007+4076C>A	ENSP00000283228.2:n.1007+4076C>A
ENST00000342084.8:c.671+4076C>A	ENSP00000339605.4:n.671+4076C>A
ENST00000378778.5:c.389+4076C>A	ENSP00000368054.1:n.389+4076C>A
ENST00000440835.6:c.272+4076C>A	ENSP00000391750.2:n.272+4076C>A
ENST00000548220.1:n.555+4076C>A
ENST00000549308.5:c.272+4076C>A	ENSP00000446943.1:n.272+4076C>A
ENST00000550661.1:c.272+4076C>A	ENSP00000449616.1:n.272+4076C>A
ENST00000551219.5:c.-10+4076C>A	ENSP00000448049.1:n.-10+4076C>A
NM_001207015.1:c.671+4076C>A	NP_001193944.1:n.671+4076C>A
NM_001207016.1:c.389+4076C>A	NP_001193945.1:n.389+4076C>A
NM_002849.3:c.1007+4076C>A	NP_002840.2:n.1007+4076C>A
NM_130846.2:c.272+4076C>A	NP_570897.2:n.272+4076C>A
NR_073474.1:n.687+4076C>A
XM_011538615.1:c.983+4076C>A	XP_011536917.1:n.983+4076C>A
XM_011538616.1:c.1007+4076C>A	XP_011536918.1:n.1007+4076C>A
XR_944652.1:n.1395+4076C>A
XR_945079.1:n.484+21919G>T
XM_011538615.2:c.983+4076C>A	XP_011536917.1:n.983+4076C>A
XR_001748830.1:n.1349+4076C>A
XR_001748831.2:n.790+4076C>A
NM_002849.4:c.1007+4076C>A MANE Select	NP_002840.2:n.1007+4076C>A
NM_001207015.2:c.671+4076C>A	NP_001193944.1:n.671+4076C>A
NM_130846.3:c.272+4076C>A	NP_570897.2:n.272+4076C>A
NR_073474.2:n.687+4076C>A