Canonical Allele Identifier: CA2739275520

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198702523_198702524delinsTG , CM000663.2:g.198702523_198702524delinsTG	GRCh38
NC_000001.10:g.198671652_198671653delinsTG , CM000663.1:g.198671652_198671653delinsTG	GRCh37
NC_000001.9:g.196938275_196938276delinsTG	NCBI36
NG_007730.1:g.68428_68429delinsTG
NG_007730.2:g.68429_68430delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.187-775_187-774delinsTG
ENST00000697631.1:c.299-775_299-774delinsTG	ENSP00000513363.1:n.299-775_299-774delinsTG
ENST00000697632.1:c.-455-775_-455-774delinsTG	ENSP00000513364.1:n.-455-775_-455-774delinsTG
ENST00000348564.11:c.101-775_101-774delinsTG	ENSP00000306782.7:n.101-775_101-774delinsTG
ENST00000367379.6:c.101-775_101-774delinsTG	ENSP00000356349.2:n.101-775_101-774delinsTG
ENST00000442510.8:c.576_577delinsTG MANE Select	ENSP00000411355.3:p.Thr193Ala
ENST00000643513.1:c.242-775_242-774delinsTG	ENSP00000494132.1:n.242-775_242-774delinsTG
ENST00000645247.1:c.365-775_365-774delinsTG	ENSP00000494327.1:n.365-775_365-774delinsTG
ENST00000348564.10:c.101-775_101-774delinsTG	ENSP00000306782.7:n.101-775_101-774delinsTG
ENST00000367367.8:c.378_379delinsTG	ENSP00000356337.5:p.Thr127Ala
ENST00000367379.5:c.101-775_101-774delinsTG	ENSP00000356349.2:n.101-775_101-774delinsTG
ENST00000391970.3:n.352_353delinsTG
ENST00000427110.6:n.216-775_216-774delinsTG
ENST00000442510.6:c.576_577delinsTG	ENSP00000411355.3:p.Thr193Ala
ENST00000462363.6:n.350-775_350-774delinsTG
ENST00000529828.5:c.440-775_440-774delinsTG	ENSP00000469141.1:n.440-775_440-774delinsTG
ENST00000530727.5:c.242-775_242-774delinsTG	ENSP00000433536.2:n.242-775_242-774delinsTG
NM_002838.4:c.576_577delinsTG	NP_002829.3:p.Thr193Ala
NM_080921.3:c.101-775_101-774delinsTG	NP_563578.2:n.101-775_101-774delinsTG
XM_006711472.2:c.440-775_440-774delinsTG	XP_006711535.1:n.440-775_440-774delinsTG
XM_006711473.2:c.378_379delinsTG	XP_006711536.1:p.Thr127Ala
XM_006711474.2:c.242-775_242-774delinsTG	XP_006711537.1:n.242-775_242-774delinsTG
XM_006711472.4:c.440-775_440-774delinsTG	XP_006711535.1:n.440-775_440-774delinsTG
XM_006711473.3:c.378_379delinsTG	XP_006711536.1:p.Thr127Ala
XM_006711474.3:c.242-775_242-774delinsTG	XP_006711537.1:n.242-775_242-774delinsTG
NM_002838.5:c.576_577delinsTG MANE Select	NP_002829.3:p.Thr193Ala
NM_080921.4:c.101-775_101-774delinsTG	NP_563578.2:n.101-775_101-774delinsTG