Canonical Allele Identifier: CA1315080

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198735169C>T , CM000663.2:g.198735169C>T	GRCh38
NC_000001.10:g.198704298C>T , CM000663.1:g.198704298C>T	GRCh37
NC_000001.9:g.196970921C>T	NCBI36
NG_007730.1:g.101074C>T
NG_007730.2:g.101075C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.1373C>T
ENST00000697630.1:n.6150C>T
ENST00000697631.1:c.2035C>T	ENSP00000513363.1:p.Arg679Trp
ENST00000697632.1:c.1282C>T	ENSP00000513364.1:p.Arg428Trp
ENST00000697633.1:c.927C>T
ENST00000348564.11:c.1837C>T	ENSP00000306782.7:p.Arg613Trp
ENST00000442510.8:c.2320C>T MANE Select	ENSP00000411355.3:p.Arg774Trp
ENST00000348564.10:c.1837C>T	ENSP00000306782.7:p.Arg613Trp
ENST00000367367.8:c.2122C>T	ENSP00000356337.5:p.Arg708Trp
ENST00000442510.6:c.2320C>T	ENSP00000411355.3:p.Arg774Trp
ENST00000529828.5:c.2176C>T	ENSP00000469141.1:p.Arg726Trp
NM_002838.4:c.2320C>T	NP_002829.3:p.Arg774Trp
NM_080921.3:c.1837C>T	NP_563578.2:p.Arg613Trp
XM_006711472.2:c.2176C>T	XP_006711535.1:p.Arg726Trp
XM_006711473.2:c.2122C>T	XP_006711536.1:p.Arg708Trp
XM_006711474.2:c.1978C>T	XP_006711537.1:p.Arg660Trp
XM_006711472.4:c.2176C>T	XP_006711535.1:p.Arg726Trp
XM_006711473.3:c.2122C>T	XP_006711536.1:p.Arg708Trp
XM_006711474.3:c.1978C>T	XP_006711537.1:p.Arg660Trp
NM_002838.5:c.2320C>T MANE Select	NP_002829.3:p.Arg774Trp
NM_080921.4:c.1837C>T	NP_563578.2:p.Arg613Trp