Canonical Allele Identifier: CA2049280237

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80506078T= , CM000674.2:g.80506078T=	GRCh38
NC_000012.11:g.80899857T= , CM000674.1:g.80899857T=	GRCh37
NC_000012.10:g.79423988T=	NCBI36
NG_034052.1:g.66733T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001145026.2:c.2327T= MANE Select	NP_001138498.1:p.Ile776=
ENST00000644991.3:c.2327T= MANE Select	ENSP00000495607.1:p.Ile776=
NM_001145026.1:c.2327T=	NP_001138498.1:p.Ile776=
ENST00000614701.4:c.2327T=	ENSP00000482885.1:p.Ile776=
ENST00000616559.4:c.2453T=	ENSP00000483259.1:p.Ile818=
XM_011538290.1:c.2327T=	XP_011536592.1:p.Ile776=
XM_017019273.1:c.2993T=	XP_016874762.1:p.Ile998=
XM_017019274.1:c.2993T=	XP_016874763.1:p.Ile998=
XM_017019275.1:c.2993T=	XP_016874764.1:p.Ile998=
XR_001748688.1:n.3130T=
XR_001748689.1:n.3130T=
XR_945144.1:n.737+7256A=