Canonical Allele Identifier: CA2588321177
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

gnomAD v4: 19-10115003-AAAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115006_10115008del , CM000681.2:g.10115006_10115008del GRCh38
NC_000019.9:g.10225682_10225684del , CM000681.1:g.10225682_10225684del GRCh37
NC_000019.8:g.10086682_10086684del NCBI36
NG_047007.1:g.8486_8488del
NG_051197.1:g.9919_9921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*268_*270del (P2RY11) MANE Select ENSP00000323872.4:n.*268_*270del
ENST00000321826.4:c.*268_*270del (P2RY11) ENSP00000323872.4:n.*268_*270del
NM_001040664.2:c.*268_*270del (PPAN-P2RY11) NP_001035754.1:n.*268_*270del
NM_001198690.1:c.*1152_*1154del (PPAN-P2RY11) NP_001185619.1:n.*1152_*1154del
NM_002566.4:c.*268_*270del (P2RY11) NP_002557.2:n.*268_*270del
NM_002566.5:c.*268_*270del (P2RY11) MANE Select NP_002557.2:n.*268_*270del
NM_001040664.3:c.*268_*270del (PPAN-P2RY11) NP_001035754.1:n.*268_*270del
NM_001198690.2:c.*1152_*1154del (PPAN-P2RY11) NP_001185619.1:n.*1152_*1154del
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