Canonical Allele Identifier: CA2322269882
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114925T= , CM000681.2:g.10114925T= GRCh38
NC_000019.9:g.10225601T= , CM000681.1:g.10225601T= GRCh37
NC_000019.8:g.10086601T= NCBI36
NG_047007.1:g.8405T=
NG_051197.1:g.10000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*187T= (P2RY11) MANE Select ENSP00000323872.4:n.*187T=
ENST00000321826.4:c.*187T= (P2RY11) ENSP00000323872.4:n.*187T=
NM_001040664.2:c.*187T= (PPAN-P2RY11) NP_001035754.1:n.*187T=
NM_001198690.1:c.*1071T= (PPAN-P2RY11) NP_001185619.1:n.*1071T=
NM_002566.4:c.*187T= (P2RY11) NP_002557.2:n.*187T=
NM_002566.5:c.*187T= (P2RY11) MANE Select NP_002557.2:n.*187T=
NM_001040664.3:c.*187T= (PPAN-P2RY11) NP_001035754.1:n.*187T=
NM_001198690.2:c.*1071T= (PPAN-P2RY11) NP_001185619.1:n.*1071T=