Canonical Allele Identifier: CA1314500

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198702343G>A , CM000663.2:g.198702343G>A	GRCh38
NC_000001.10:g.198671472G>A , CM000663.1:g.198671472G>A	GRCh37
NC_000001.9:g.196938095G>A	NCBI36
NG_007730.1:g.68248G>A
NG_007730.2:g.68249G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.187-955G>A
ENST00000697631.1:c.299-955G>A	ENSP00000513363.1:n.299-955G>A
ENST00000697632.1:c.-455-955G>A	ENSP00000513364.1:n.-455-955G>A
ENST00000348564.11:c.101-955G>A	ENSP00000306782.7:n.101-955G>A
ENST00000367379.6:c.101-955G>A	ENSP00000356349.2:n.101-955G>A
ENST00000442510.8:c.440-44G>A MANE Select	ENSP00000411355.3:n.440-44G>A
ENST00000643513.1:c.242-955G>A	ENSP00000494132.1:n.242-955G>A
ENST00000645247.1:c.365-955G>A	ENSP00000494327.1:n.365-955G>A
ENST00000348564.10:c.101-955G>A	ENSP00000306782.7:n.101-955G>A
ENST00000367367.8:c.242-44G>A	ENSP00000356337.5:n.242-44G>A
ENST00000367379.5:c.101-955G>A	ENSP00000356349.2:n.101-955G>A
ENST00000391970.3:n.216-44G>A
ENST00000427110.6:n.216-955G>A
ENST00000442510.6:c.440-44G>A	ENSP00000411355.3:n.440-44G>A
ENST00000462363.6:n.350-955G>A
ENST00000529828.5:c.440-955G>A	ENSP00000469141.1:n.440-955G>A
ENST00000530727.5:c.242-955G>A	ENSP00000433536.2:n.242-955G>A
NM_002838.4:c.440-44G>A	NP_002829.3:n.440-44G>A
NM_080921.3:c.101-955G>A	NP_563578.2:n.101-955G>A
XM_006711472.2:c.440-955G>A	XP_006711535.1:n.440-955G>A
XM_006711473.2:c.242-44G>A	XP_006711536.1:n.242-44G>A
XM_006711474.2:c.242-955G>A	XP_006711537.1:n.242-955G>A
XM_006711472.4:c.440-955G>A	XP_006711535.1:n.440-955G>A
XM_006711473.3:c.242-44G>A	XP_006711536.1:n.242-44G>A
XM_006711474.3:c.242-955G>A	XP_006711537.1:n.242-955G>A
NM_002838.5:c.440-44G>A MANE Select	NP_002829.3:n.440-44G>A
NM_080921.4:c.101-955G>A	NP_563578.2:n.101-955G>A