Canonical Allele Identifier: CA606303801

Gene: PTPRQ

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80669473_80669476dup , CM000674.2:g.80669473_80669476dup	GRCh38
NC_000012.11:g.81063252_81063255dup , CM000674.1:g.81063252_81063255dup	GRCh37
NC_000012.10:g.79587383_79587386dup	NCBI36
NG_034052.1:g.230128_230131dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.6453+9_6453+12dup MANE Select	ENSP00000495607.1:n.6453+9_6453+12dup
ENST00000614701.4:c.6453+9_6453+12dup	ENSP00000482885.1:n.6453+9_6453+12dup
ENST00000616559.4:c.6552+9_6552+12dup	ENSP00000483259.1:n.6552+9_6552+12dup
NM_001145026.1:c.6453+9_6453+12dup	NP_001138498.1:n.6453+9_6453+12dup
XM_011538290.1:c.6519+9_6519+12dup	XP_011536592.1:n.6519+9_6519+12dup
XR_945142.1:n.111-22722_111-22719dup
XM_017019273.1:c.7164+9_7164+12dup	XP_016874762.1:n.7164+9_7164+12dup
XM_017019274.1:c.7119+9_7119+12dup	XP_016874763.1:n.7119+9_7119+12dup
XR_001749222.1:n.120+37639_120+37642dup
NM_001145026.2:c.6453+9_6453+12dup MANE Select	NP_001138498.1:n.6453+9_6453+12dup