Canonical Allele Identifier: CA2588321180
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115006_10115009del , CM000681.2:g.10115006_10115009del GRCh38
NC_000019.9:g.10225682_10225685del , CM000681.1:g.10225682_10225685del GRCh37
NC_000019.8:g.10086682_10086685del NCBI36
NG_047007.1:g.8486_8489del
NG_051197.1:g.9916_9919del

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*268_*271del (P2RY11) MANE Select ENSP00000323872.4:n.*268_*271del
ENST00000321826.4:c.*268_*271del (P2RY11) ENSP00000323872.4:n.*268_*271del
NM_001040664.2:c.*268_*271del (PPAN-P2RY11) NP_001035754.1:n.*268_*271del
NM_001198690.1:c.*1152_*1155del (PPAN-P2RY11) NP_001185619.1:n.*1152_*1155del
NM_002566.4:c.*268_*271del (P2RY11) NP_002557.2:n.*268_*271del
NM_002566.5:c.*268_*271del (P2RY11) MANE Select NP_002557.2:n.*268_*271del
NM_001040664.3:c.*268_*271del (PPAN-P2RY11) NP_001035754.1:n.*268_*271del
NM_001198690.2:c.*1152_*1155del (PPAN-P2RY11) NP_001185619.1:n.*1152_*1155del