Canonical Allele Identifier: CA35893481
Community Standard Title: NM_002838.5(PTPRC):c.1451-64T>C
Gene: PTPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198718030T>C , CM000663.2:g.198718030T>C GRCh38
NC_000001.10:g.198687159T>C , CM000663.1:g.198687159T>C GRCh37
NC_000001.9:g.196953782T>C NCBI36
NG_007730.1:g.83935T>C
NG_007730.2:g.83936T>C

Transcript Alleles

HGVS Amino-acid Change
NM_002838.5:c.1451-64T>C MANE Select NP_002829.3:n.1451-64T>C
ENST00000442510.8:c.1451-64T>C MANE Select ENSP00000411355.3:n.1451-64T>C
NM_002838.4:c.1451-64T>C NP_002829.3:n.1451-64T>C
NM_080921.3:c.968-64T>C NP_563578.2:n.968-64T>C
NM_080921.4:c.968-64T>C NP_563578.2:n.968-64T>C
ENST00000348564.10:c.968-64T>C ENSP00000306782.7:n.968-64T>C
ENST00000348564.11:c.968-64T>C ENSP00000306782.7:n.968-64T>C
ENST00000367367.8:c.1253-64T>C ENSP00000356337.5:n.1253-64T>C
ENST00000442510.6:c.1451-64T>C ENSP00000411355.3:n.1451-64T>C
ENST00000491302.1:n.443-64T>C
ENST00000491302.2:n.504-64T>C
ENST00000529828.5:c.1307-64T>C ENSP00000469141.1:n.1307-64T>C
ENST00000530727.5:c.1109-64T>C ENSP00000433536.2:n.1109-64T>C
ENST00000697630.1:n.5281-64T>C
ENST00000697631.1:c.1166-64T>C ENSP00000513363.1:n.1166-64T>C
ENST00000697632.1:c.413-64T>C ENSP00000513364.1:n.413-64T>C
XM_006711472.2:c.1307-64T>C XP_006711535.1:n.1307-64T>C
XM_006711472.4:c.1307-64T>C XP_006711535.1:n.1307-64T>C
XM_006711473.2:c.1253-64T>C XP_006711536.1:n.1253-64T>C
XM_006711473.3:c.1253-64T>C XP_006711536.1:n.1253-64T>C
XM_006711474.2:c.1109-64T>C XP_006711537.1:n.1109-64T>C
XM_006711474.3:c.1109-64T>C XP_006711537.1:n.1109-64T>C