Canonical Allele Identifier: CA16603468
Gene: PTPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198706804A>C , CM000663.2:g.198706804A>C GRCh38
NC_000001.10:g.198675933A>C , CM000663.1:g.198675933A>C GRCh37
NC_000001.9:g.196942556A>C NCBI36
NG_007730.1:g.72709A>C
NG_007730.2:g.72710A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697630.1:n.1458A>C
ENST00000697631.1:c.471A>C ENSP00000513363.1:p.Leu157=
ENST00000697632.1:c.-283A>C ENSP00000513364.1:n.-283A>C
ENST00000348564.11:c.273A>C ENSP00000306782.7:p.Leu91=
ENST00000367379.6:c.273A>C ENSP00000356349.2:p.Leu91=
ENST00000442510.8:c.756A>C MANE Select ENSP00000411355.3:p.Leu252=
ENST00000643513.1:c.414A>C ENSP00000494132.1:p.Leu138=
ENST00000348564.10:c.273A>C ENSP00000306782.7:p.Leu91=
ENST00000367367.8:c.558A>C ENSP00000356337.5:p.Leu186=
ENST00000367379.5:c.273A>C ENSP00000356349.2:p.Leu91=
ENST00000442510.6:c.756A>C ENSP00000411355.3:p.Leu252=
ENST00000529828.5:c.612A>C ENSP00000469141.1:p.Leu204=
ENST00000530727.5:c.414A>C ENSP00000433536.2:p.Leu138=
NM_002838.4:c.756A>C NP_002829.3:p.Leu252=
NM_080921.3:c.273A>C NP_563578.2:p.Leu91=
XM_006711472.2:c.612A>C XP_006711535.1:p.Leu204=
XM_006711473.2:c.558A>C XP_006711536.1:p.Leu186=
XM_006711474.2:c.414A>C XP_006711537.1:p.Leu138=
XM_006711472.4:c.612A>C XP_006711535.1:p.Leu204=
XM_006711473.3:c.558A>C XP_006711536.1:p.Leu186=
XM_006711474.3:c.414A>C XP_006711537.1:p.Leu138=
NM_002838.5:c.756A>C MANE Select NP_002829.3:p.Leu252=
NM_080921.4:c.273A>C NP_563578.2:p.Leu91=