Canonical Allele Identifier: CA2813565507
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114823_10114824insTGAG , CM000681.2:g.10114823_10114824insTGAG GRCh38
NC_000019.9:g.10225499_10225500insTGAG , CM000681.1:g.10225499_10225500insTGAG GRCh37
NC_000019.8:g.10086499_10086500insTGAG NCBI36
NG_047007.1:g.8303_8304insTGAG
NG_051197.1:g.10101_10102insCTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*85_*86insTGAG (P2RY11) MANE Select ENSP00000323872.4:n.*85_*86insTGAG
ENST00000321826.4:c.*85_*86insTGAG (P2RY11) ENSP00000323872.4:n.*85_*86insTGAG
NM_001040664.2:c.*85_*86insTGAG (PPAN-P2RY11) NP_001035754.1:n.*85_*86insTGAG
NM_001198690.1:c.*969_*970insTGAG (PPAN-P2RY11) NP_001185619.1:n.*969_*970insTGAG
NM_002566.4:c.*85_*86insTGAG (P2RY11) NP_002557.2:n.*85_*86insTGAG
NM_002566.5:c.*85_*86insTGAG (P2RY11) MANE Select NP_002557.2:n.*85_*86insTGAG
NM_001040664.3:c.*85_*86insTGAG (PPAN-P2RY11) NP_001035754.1:n.*85_*86insTGAG
NM_001198690.2:c.*969_*970insTGAG (PPAN-P2RY11) NP_001185619.1:n.*969_*970insTGAG
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