Canonical Allele Identifier: CA2049256754

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460604_80460605delinsAC , CM000674.2:g.80460604_80460605delinsAC	GRCh38
NC_000012.11:g.80849572_80849573delinsGT , CM000674.1:g.80849572_80849573delinsGT	GRCh37
NC_000012.10:g.79373703_79373704delinsGT	NCBI36
NG_034052.1:g.21259_21260delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.661-49_661-48delinsAC MANE Select	ENSP00000495607.1:n.661-49_661-48delinsAC
ENST00000614701.4:c.661-49_661-48delinsAC	ENSP00000482885.1:n.661-49_661-48delinsAC
ENST00000616559.4:c.787-49_787-48delinsAC	ENSP00000483259.1:n.787-49_787-48delinsAC
NM_001145026.1:c.661-49_661-48delinsAC	NP_001138498.1:n.661-49_661-48delinsAC
XM_011538290.1:c.661-49_661-48delinsAC	XP_011536592.1:n.661-49_661-48delinsAC
XM_017019273.1:c.1327-49_1327-48delinsAC	XP_016874762.1:n.1327-49_1327-48delinsAC
XM_017019274.1:c.1327-49_1327-48delinsAC	XP_016874763.1:n.1327-49_1327-48delinsAC
XM_017019275.1:c.1327-49_1327-48delinsAC	XP_016874764.1:n.1327-49_1327-48delinsAC
XR_001748688.1:n.1464-49_1464-48delinsAC
XR_001748689.1:n.1464-49_1464-48delinsAC
NM_001145026.2:c.661-49_661-48delinsAC MANE Select	NP_001138498.1:n.661-49_661-48delinsAC