Canonical Allele Identifier: CA2322269932
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114986T= , CM000681.2:g.10114986T= GRCh38
NC_000019.9:g.10225662T= , CM000681.1:g.10225662T= GRCh37
NC_000019.8:g.10086662T= NCBI36
NG_047007.1:g.8466T=
NG_051197.1:g.9939A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*248T= (P2RY11) MANE Select ENSP00000323872.4:n.*248T=
ENST00000321826.4:c.*248T= (P2RY11) ENSP00000323872.4:n.*248T=
NM_001040664.2:c.*248T= (PPAN-P2RY11) NP_001035754.1:n.*248T=
NM_001198690.1:c.*1132T= (PPAN-P2RY11) NP_001185619.1:n.*1132T=
NM_002566.4:c.*248T= (P2RY11) NP_002557.2:n.*248T=
NM_002566.5:c.*248T= (P2RY11) MANE Select NP_002557.2:n.*248T=
NM_001040664.3:c.*248T= (PPAN-P2RY11) NP_001035754.1:n.*248T=
NM_001198690.2:c.*1132T= (PPAN-P2RY11) NP_001185619.1:n.*1132T=