Canonical Allele Identifier: CA2620023713

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80484402-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484402_80484403insA , CM000674.2:g.80484402_80484403insA	GRCh38
NC_000012.11:g.80878181_80878182insA , CM000674.1:g.80878181_80878182insA	GRCh37
NC_000012.10:g.79402312_79402313insA	NCBI36
NG_034052.1:g.45057_45058insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1187-31_1187-30insA MANE Select	ENSP00000495607.1:n.1187-31_1187-30insA
ENST00000614701.4:c.1187-31_1187-30insA	ENSP00000482885.1:n.1187-31_1187-30insA
ENST00000616559.4:c.1313-31_1313-30insA	ENSP00000483259.1:n.1313-31_1313-30insA
NM_001145026.1:c.1187-31_1187-30insA	NP_001138498.1:n.1187-31_1187-30insA
XM_011538290.1:c.1187-31_1187-30insA	XP_011536592.1:n.1187-31_1187-30insA
XM_017019273.1:c.1853-31_1853-30insA	XP_016874762.1:n.1853-31_1853-30insA
XM_017019274.1:c.1853-31_1853-30insA	XP_016874763.1:n.1853-31_1853-30insA
XM_017019275.1:c.1853-31_1853-30insA	XP_016874764.1:n.1853-31_1853-30insA
XR_001748688.1:n.1990-31_1990-30insA
XR_001748689.1:n.1990-31_1990-30insA
NM_001145026.2:c.1187-31_1187-30insA MANE Select	NP_001138498.1:n.1187-31_1187-30insA