Canonical Allele Identifier: CA1314424

Gene: PTPRC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198696788C>T , CM000663.2:g.198696788C>T	GRCh38
NC_000001.10:g.198665917C>T , CM000663.1:g.198665917C>T	GRCh37
NC_000001.9:g.196932540C>T	NCBI36
NG_007730.1:g.62693C>T
NG_007730.2:g.62694C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697630.1:n.186+4415C>T
ENST00000697631.1:c.177C>T	ENSP00000513363.1:p.Pro59=
ENST00000697632.1:c.-456+4415C>T	ENSP00000513364.1:n.-456+4415C>T
ENST00000348564.11:c.100+4415C>T	ENSP00000306782.7:n.100+4415C>T
ENST00000367379.6:c.100+4415C>T	ENSP00000356349.2:n.100+4415C>T
ENST00000442510.8:c.177C>T MANE Select	ENSP00000411355.3:p.Pro59=
ENST00000643513.1:c.101-2776C>T	ENSP00000494132.1:n.101-2776C>T
ENST00000645247.1:c.223+2648C>T	ENSP00000494327.1:n.223+2648C>T
ENST00000348564.10:c.100+4415C>T	ENSP00000306782.7:n.100+4415C>T
ENST00000367367.8:c.101-2776C>T	ENSP00000356337.5:n.101-2776C>T
ENST00000367379.5:c.100+4415C>T	ENSP00000356349.2:n.100+4415C>T
ENST00000391970.3:n.75-2776C>T
ENST00000418674.1:c.177C>T	ENSP00000393360.2:p.Pro59=
ENST00000427110.6:n.75-2776C>T
ENST00000442510.6:c.177C>T	ENSP00000411355.3:p.Pro59=
ENST00000462363.6:n.209-2776C>T
ENST00000529828.5:c.177C>T	ENSP00000469141.1:p.Pro59=
ENST00000530727.5:c.101-2776C>T	ENSP00000433536.2:n.101-2776C>T
NM_002838.4:c.177C>T	NP_002829.3:p.Pro59=
NM_080921.3:c.100+4415C>T	NP_563578.2:n.100+4415C>T
XM_006711472.2:c.177C>T	XP_006711535.1:p.Pro59=
XM_006711473.2:c.101-2776C>T	XP_006711536.1:n.101-2776C>T
XM_006711474.2:c.101-2776C>T	XP_006711537.1:n.101-2776C>T
XM_006711472.4:c.177C>T	XP_006711535.1:p.Pro59=
XM_006711473.3:c.101-2776C>T	XP_006711536.1:n.101-2776C>T
XM_006711474.3:c.101-2776C>T	XP_006711537.1:n.101-2776C>T
NM_002838.5:c.177C>T MANE Select	NP_002829.3:p.Pro59=
NM_080921.4:c.100+4415C>T	NP_563578.2:n.100+4415C>T