Canonical Allele Identifier: CA1314607

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198706748A>G , CM000663.2:g.198706748A>G	GRCh38
NC_000001.10:g.198675877A>G , CM000663.1:g.198675877A>G	GRCh37
NC_000001.9:g.196942500A>G	NCBI36
NG_007730.1:g.72653A>G
NG_007730.2:g.72654A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002838.5:c.700A>G MANE Select	NP_002829.3:p.Asn234Asp
ENST00000442510.8:c.700A>G MANE Select	ENSP00000411355.3:p.Asn234Asp
NM_002838.4:c.700A>G	NP_002829.3:p.Asn234Asp
NM_080921.3:c.217A>G	NP_563578.2:p.Asn73Asp
NM_080921.4:c.217A>G	NP_563578.2:p.Asn73Asp
ENST00000348564.10:c.217A>G	ENSP00000306782.7:p.Asn73Asp
ENST00000348564.11:c.217A>G	ENSP00000306782.7:p.Asn73Asp
ENST00000367367.8:c.502A>G	ENSP00000356337.5:p.Asn168Asp
ENST00000367379.5:c.217A>G	ENSP00000356349.2:p.Asn73Asp
ENST00000367379.6:c.217A>G	ENSP00000356349.2:p.Asn73Asp
ENST00000442510.6:c.700A>G	ENSP00000411355.3:p.Asn234Asp
ENST00000529828.5:c.556A>G	ENSP00000469141.1:p.Asn186Asp
ENST00000530727.5:c.358A>G	ENSP00000433536.2:p.Asn120Asp
ENST00000643513.1:c.358A>G	ENSP00000494132.1:p.Asn120Asp
ENST00000697630.1:n.1402A>G
ENST00000697631.1:c.415A>G	ENSP00000513363.1:p.Asn139Asp
ENST00000697632.1:c.-339A>G	ENSP00000513364.1:n.-339A>G
XM_006711472.2:c.556A>G	XP_006711535.1:p.Asn186Asp
XM_006711472.4:c.556A>G	XP_006711535.1:p.Asn186Asp
XM_006711473.2:c.502A>G	XP_006711536.1:p.Asn168Asp
XM_006711473.3:c.502A>G	XP_006711536.1:p.Asn168Asp
XM_006711474.2:c.358A>G	XP_006711537.1:p.Asn120Asp
XM_006711474.3:c.358A>G	XP_006711537.1:p.Asn120Asp