Canonical Allele Identifier: CA2049256789

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460663_80460672delinsAATCTTTTTT , CM000674.2:g.80460663_80460672delinsAATCTTTTTT	GRCh38
NC_000012.11:g.80849505_80849514delinsAAAAAAGATT , CM000674.1:g.80849505_80849514delinsAAAAAAGATT	GRCh37
NC_000012.10:g.79373636_79373645delinsAAAAAAGATT	NCBI36
NG_034052.1:g.21318_21327delinsAATCTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.671_680delinsAATCTTTTTT MANE Select	ENSP00000495607.1:p.Glu224=
ENST00000614701.4:c.671_680delinsAATCTTTTTT	ENSP00000482885.1:p.Glu224=
ENST00000616559.4:c.797_806delinsAATCTTTTTT	ENSP00000483259.1:p.Glu266=
NM_001145026.1:c.671_680delinsAATCTTTTTT	NP_001138498.1:p.Glu224=
XM_011538290.1:c.671_680delinsAATCTTTTTT	XP_011536592.1:p.Glu224=
XM_017019273.1:c.1337_1346delinsAATCTTTTTT	XP_016874762.1:p.Glu446=
XM_017019274.1:c.1337_1346delinsAATCTTTTTT	XP_016874763.1:p.Glu446=
XM_017019275.1:c.1337_1346delinsAATCTTTTTT	XP_016874764.1:p.Glu446=
XR_001748688.1:n.1474_1483delinsAATCTTTTTT
XR_001748689.1:n.1474_1483delinsAATCTTTTTT
NM_001145026.2:c.671_680delinsAATCTTTTTT MANE Select	NP_001138498.1:p.Glu224=