Canonical Allele Identifier: CA2322269815
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs566432369

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114827A>C , CM000681.2:g.10114827A>C GRCh38
NC_000019.9:g.10225503A>C , CM000681.1:g.10225503A>C GRCh37
NC_000019.8:g.10086503A>C NCBI36
NG_047007.1:g.8307A>C
NG_051197.1:g.10098T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*89A>C (P2RY11) MANE Select ENSP00000323872.4:n.*89A>C
ENST00000321826.4:c.*89A>C (P2RY11) ENSP00000323872.4:n.*89A>C
NM_001040664.2:c.*89A>C (PPAN-P2RY11) NP_001035754.1:n.*89A>C
NM_001198690.1:c.*973A>C (PPAN-P2RY11) NP_001185619.1:n.*973A>C
NM_002566.4:c.*89A>C (P2RY11) NP_002557.2:n.*89A>C
NM_002566.5:c.*89A>C (P2RY11) MANE Select NP_002557.2:n.*89A>C
NM_001040664.3:c.*89A>C (PPAN-P2RY11) NP_001035754.1:n.*89A>C
NM_001198690.2:c.*973A>C (PPAN-P2RY11) NP_001185619.1:n.*973A>C