Canonical Allele Identifier: CA2322269938
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114995A= , CM000681.2:g.10114995A= GRCh38
NC_000019.9:g.10225671A= , CM000681.1:g.10225671A= GRCh37
NC_000019.8:g.10086671A= NCBI36
NG_047007.1:g.8475A=
NG_051197.1:g.9930T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*257A= (P2RY11) MANE Select ENSP00000323872.4:n.*257A=
ENST00000321826.4:c.*257A= (P2RY11) ENSP00000323872.4:n.*257A=
NM_001040664.2:c.*257A= (PPAN-P2RY11) NP_001035754.1:n.*257A=
NM_001198690.1:c.*1141A= (PPAN-P2RY11) NP_001185619.1:n.*1141A=
NM_002566.4:c.*257A= (P2RY11) NP_002557.2:n.*257A=
NM_002566.5:c.*257A= (P2RY11) MANE Select NP_002557.2:n.*257A=
NM_001040664.3:c.*257A= (PPAN-P2RY11) NP_001035754.1:n.*257A=
NM_001198690.2:c.*1141A= (PPAN-P2RY11) NP_001185619.1:n.*1141A=
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