Canonical Allele Identifier: CA2582339941
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

gnomAD v3: 19-10114850-GCCAGGTCAGGCCCAGCTGCAGCC-G
gnomAD v4: 19-10114850-GCCAGGTCAGGCCCAGCTGCAGCC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114852_10114874del , CM000681.2:g.10114852_10114874del GRCh38
NC_000019.9:g.10225528_10225550del , CM000681.1:g.10225528_10225550del GRCh37
NC_000019.8:g.10086528_10086550del NCBI36
NG_047007.1:g.8332_8354del
NG_051197.1:g.10052_10074del

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*114_*136del (P2RY11) MANE Select ENSP00000323872.4:n.*114_*136del
ENST00000321826.4:c.*114_*136del (P2RY11) ENSP00000323872.4:n.*114_*136del
NM_001040664.2:c.*114_*136del (PPAN-P2RY11) NP_001035754.1:n.*114_*136del
NM_001198690.1:c.*998_*1020del (PPAN-P2RY11) NP_001185619.1:n.*998_*1020del
NM_002566.4:c.*114_*136del (P2RY11) NP_002557.2:n.*114_*136del
NM_002566.5:c.*114_*136del (P2RY11) MANE Select NP_002557.2:n.*114_*136del
NM_001040664.3:c.*114_*136del (PPAN-P2RY11) NP_001035754.1:n.*114_*136del
NM_001198690.2:c.*998_*1020del (PPAN-P2RY11) NP_001185619.1:n.*998_*1020del
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