Canonical Allele Identifier: CA239462119

Gene: PTPRR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.70895776G>A , CM000674.2:g.70895776G>A	GRCh38
NC_000012.11:g.71289556G>A , CM000674.1:g.71289556G>A	GRCh37
NC_000012.10:g.69575823G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283228.7:c.59-2799C>T MANE Select	ENSP00000283228.2:n.59-2799C>T
ENST00000283228.6:c.59-2799C>T	ENSP00000283228.2:n.59-2799C>T
NM_002849.3:c.59-2799C>T	NP_002840.2:n.59-2799C>T
XM_011538615.1:c.35-2799C>T	XP_011536917.1:n.35-2799C>T
XM_011538616.1:c.59-2799C>T	XP_011536918.1:n.59-2799C>T
XR_944652.1:n.447-2799C>T
XM_011538615.2:c.35-2799C>T	XP_011536917.1:n.35-2799C>T
XR_001748830.1:n.401-2799C>T
NM_002849.4:c.59-2799C>T MANE Select	NP_002840.2:n.59-2799C>T