Canonical Allele Identifier: CA2588321134
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

gnomAD v4: 19-10114960-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114960G>A , CM000681.2:g.10114960G>A GRCh38
NC_000019.9:g.10225636G>A , CM000681.1:g.10225636G>A GRCh37
NC_000019.8:g.10086636G>A NCBI36
NG_047007.1:g.8440G>A
NG_051197.1:g.9965C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*222G>A (P2RY11) MANE Select ENSP00000323872.4:n.*222G>A
ENST00000321826.4:c.*222G>A (P2RY11) ENSP00000323872.4:n.*222G>A
NM_001040664.2:c.*222G>A (PPAN-P2RY11) NP_001035754.1:n.*222G>A
NM_001198690.1:c.*1106G>A (PPAN-P2RY11) NP_001185619.1:n.*1106G>A
NM_002566.4:c.*222G>A (P2RY11) NP_002557.2:n.*222G>A
NM_002566.5:c.*222G>A (P2RY11) MANE Select NP_002557.2:n.*222G>A
NM_001040664.3:c.*222G>A (PPAN-P2RY11) NP_001035754.1:n.*222G>A
NM_001198690.2:c.*1106G>A (PPAN-P2RY11) NP_001185619.1:n.*1106G>A
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