Canonical Allele Identifier: CA783165568

Gene: P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs1205682112
• MyVariant Identifiers: chr19:g.10225525A>T (hg19) ; chr19:g.10114849A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10114849A>T , CM000681.2:g.10114849A>T	GRCh38
NC_000019.9:g.10225525A>T , CM000681.1:g.10225525A>T	GRCh37
NC_000019.8:g.10086525A>T	NCBI36
NG_047007.1:g.8329A>T
NG_051197.1:g.10076T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321826.5:c.*111A>T (P2RY11) MANE Select	ENSP00000323872.4:n.*111A>T
ENST00000321826.4:c.*111A>T (P2RY11)	ENSP00000323872.4:n.*111A>T
NM_001040664.2:c.*111A>T (PPAN-P2RY11)	NP_001035754.1:n.*111A>T
NM_001198690.1:c.*995A>T (PPAN-P2RY11)	NP_001185619.1:n.*995A>T
NM_002566.4:c.*111A>T (P2RY11)	NP_002557.2:n.*111A>T
NM_002566.5:c.*111A>T (P2RY11) MANE Select	NP_002557.2:n.*111A>T
NM_001040664.3:c.*111A>T (PPAN-P2RY11)	NP_001035754.1:n.*111A>T
NM_001198690.2:c.*995A>T (PPAN-P2RY11)	NP_001185619.1:n.*995A>T