Canonical Allele Identifier: CA2588321074
Gene: P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs2145224027

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10114910G>A , CM000681.2:g.10114910G>A GRCh38
NC_000019.9:g.10225586G>A , CM000681.1:g.10225586G>A GRCh37
NC_000019.8:g.10086586G>A NCBI36
NG_047007.1:g.8390G>A
NG_051197.1:g.10015C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000321826.5:c.*172G>A (P2RY11) MANE Select ENSP00000323872.4:n.*172G>A
ENST00000321826.4:c.*172G>A (P2RY11) ENSP00000323872.4:n.*172G>A
NM_001040664.2:c.*172G>A (PPAN-P2RY11) NP_001035754.1:n.*172G>A
NM_001198690.1:c.*1056G>A (PPAN-P2RY11) NP_001185619.1:n.*1056G>A
NM_002566.4:c.*172G>A (P2RY11) NP_002557.2:n.*172G>A
NM_002566.5:c.*172G>A (P2RY11) MANE Select NP_002557.2:n.*172G>A
NM_001040664.3:c.*172G>A (PPAN-P2RY11) NP_001035754.1:n.*172G>A
NM_001198690.2:c.*1056G>A (PPAN-P2RY11) NP_001185619.1:n.*1056G>A