Canonical Allele Identifier: CA292978

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198752665C>T , CM000663.2:g.198752665C>T	GRCh38
NC_000001.10:g.198721794C>T , CM000663.1:g.198721794C>T	GRCh37
NC_000001.9:g.196988417C>T	NCBI36
NG_007730.1:g.118570C>T
NG_007730.2:g.118571C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.2455C>T
ENST00000697631.1:c.3117C>T	ENSP00000513363.1:p.Pro1039=
ENST00000697632.1:c.2364C>T	ENSP00000513364.1:p.Pro788=
ENST00000697633.1:c.2009C>T
ENST00000697634.1:n.1559C>T
ENST00000697635.1:n.355C>T
ENST00000348564.11:c.2919C>T	ENSP00000306782.7:p.Pro973=
ENST00000442510.8:c.3402C>T MANE Select	ENSP00000411355.3:p.Pro1134=
ENST00000646230.1:n.311C>T
ENST00000348564.10:c.2919C>T	ENSP00000306782.7:p.Pro973=
ENST00000442510.6:c.3402C>T	ENSP00000411355.3:p.Pro1134=
NM_002838.4:c.3402C>T	NP_002829.3:p.Pro1134=
NM_080921.3:c.2919C>T	NP_563578.2:p.Pro973=
XM_006711472.2:c.3258C>T	XP_006711535.1:p.Pro1086=
XM_006711473.2:c.3204C>T	XP_006711536.1:p.Pro1068=
XM_006711474.2:c.3060C>T	XP_006711537.1:p.Pro1020=
XM_006711472.4:c.3258C>T	XP_006711535.1:p.Pro1086=
XM_006711473.3:c.3204C>T	XP_006711536.1:p.Pro1068=
XM_006711474.3:c.3060C>T	XP_006711537.1:p.Pro1020=
NM_002838.5:c.3402C>T MANE Select	NP_002829.3:p.Pro1134=
NM_080921.4:c.2919C>T	NP_563578.2:p.Pro973=