Canonical Allele Identifier: CA2322269949
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs2089213530

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115007A>C , CM000681.2:g.10115007A>C GRCh38
NC_000019.9:g.10225683A>C , CM000681.1:g.10225683A>C GRCh37
NC_000019.8:g.10086683A>C NCBI36
NG_047007.1:g.8487A>C
NG_051197.1:g.9918T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*269A>C (P2RY11) MANE Select ENSP00000323872.4:n.*269A>C
ENST00000321826.4:c.*269A>C (P2RY11) ENSP00000323872.4:n.*269A>C
NM_001040664.2:c.*269A>C (PPAN-P2RY11) NP_001035754.1:n.*269A>C
NM_001198690.1:c.*1153A>C (PPAN-P2RY11) NP_001185619.1:n.*1153A>C
NM_002566.4:c.*269A>C (P2RY11) NP_002557.2:n.*269A>C
NM_002566.5:c.*269A>C (P2RY11) MANE Select NP_002557.2:n.*269A>C
NM_001040664.3:c.*269A>C (PPAN-P2RY11) NP_001035754.1:n.*269A>C
NM_001198690.2:c.*1153A>C (PPAN-P2RY11) NP_001185619.1:n.*1153A>C