Canonical Allele Identifier: CA1218611776
Gene: PTPRC HGNC NCBI

Linked Data

dbSNP Id: rs10919563

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198731313G>T , CM000663.2:g.198731313G>T GRCh38
NC_000001.10:g.198700442G>T , CM000663.1:g.198700442G>T GRCh37
NC_000001.9:g.196967065G>T NCBI36
NG_007730.1:g.97218G>T
NG_007730.2:g.97219G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000491302.2:n.918-304G>T
ENST00000697630.1:n.5695-304G>T
ENST00000697631.1:c.1580-304G>T ENSP00000513363.1:n.1580-304G>T
ENST00000697632.1:c.827-304G>T ENSP00000513364.1:n.827-304G>T
ENST00000697633.1:c.472-304G>T
ENST00000348564.11:c.1382-304G>T ENSP00000306782.7:n.1382-304G>T
ENST00000442510.8:c.1865-304G>T MANE Select ENSP00000411355.3:n.1865-304G>T
ENST00000348564.10:c.1382-304G>T ENSP00000306782.7:n.1382-304G>T
ENST00000367367.8:c.1667-304G>T ENSP00000356337.5:n.1667-304G>T
ENST00000442510.6:c.1865-304G>T ENSP00000411355.3:n.1865-304G>T
ENST00000529828.5:c.1721-304G>T ENSP00000469141.1:n.1721-304G>T
ENST00000530727.5:c.1523-304G>T ENSP00000433536.2:n.1523-304G>T
NM_002838.4:c.1865-304G>T NP_002829.3:n.1865-304G>T
NM_080921.3:c.1382-304G>T NP_563578.2:n.1382-304G>T
XM_006711472.2:c.1721-304G>T XP_006711535.1:n.1721-304G>T
XM_006711473.2:c.1667-304G>T XP_006711536.1:n.1667-304G>T
XM_006711474.2:c.1523-304G>T XP_006711537.1:n.1523-304G>T
XM_006711472.4:c.1721-304G>T XP_006711535.1:n.1721-304G>T
XM_006711473.3:c.1667-304G>T XP_006711536.1:n.1667-304G>T
XM_006711474.3:c.1523-304G>T XP_006711537.1:n.1523-304G>T
NM_002838.5:c.1865-304G>T MANE Select NP_002829.3:n.1865-304G>T
NM_080921.4:c.1382-304G>T NP_563578.2:n.1382-304G>T