Canonical Allele Identifier: CA2049256775

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460635_80460636delinsTC , CM000674.2:g.80460635_80460636delinsTC	GRCh38
NC_000012.11:g.80849541_80849542delinsGA , CM000674.1:g.80849541_80849542delinsGA	GRCh37
NC_000012.10:g.79373672_79373673delinsGA	NCBI36
NG_034052.1:g.21290_21291delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.661-18_661-17delinsTC MANE Select	ENSP00000495607.1:n.661-18_661-17delinsTC
ENST00000614701.4:c.661-18_661-17delinsTC	ENSP00000482885.1:n.661-18_661-17delinsTC
ENST00000616559.4:c.787-18_787-17delinsTC	ENSP00000483259.1:n.787-18_787-17delinsTC
NM_001145026.1:c.661-18_661-17delinsTC	NP_001138498.1:n.661-18_661-17delinsTC
XM_011538290.1:c.661-18_661-17delinsTC	XP_011536592.1:n.661-18_661-17delinsTC
XM_017019273.1:c.1327-18_1327-17delinsTC	XP_016874762.1:n.1327-18_1327-17delinsTC
XM_017019274.1:c.1327-18_1327-17delinsTC	XP_016874763.1:n.1327-18_1327-17delinsTC
XM_017019275.1:c.1327-18_1327-17delinsTC	XP_016874764.1:n.1327-18_1327-17delinsTC
XR_001748688.1:n.1464-18_1464-17delinsTC
XR_001748689.1:n.1464-18_1464-17delinsTC
NM_001145026.2:c.661-18_661-17delinsTC MANE Select	NP_001138498.1:n.661-18_661-17delinsTC