Canonical Allele Identifier: CA783165558

Gene: P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs1157977779
• gnomAD v4: 19-10114826-C-CA
• MyVariant Identifiers: chr19:g.10225502_10225503insA (hg19) ; chr19:g.10114826_10114827insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10114831dup , CM000681.2:g.10114831dup	GRCh38
NC_000019.9:g.10225507dup , CM000681.1:g.10225507dup	GRCh37
NC_000019.8:g.10086507dup	NCBI36
NG_047007.1:g.8311dup
NG_051197.1:g.10098dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321826.5:c.*93dup (P2RY11) MANE Select	ENSP00000323872.4:n.*93dup
ENST00000321826.4:c.*93dup (P2RY11)	ENSP00000323872.4:n.*93dup
NM_001040664.2:c.*93dup (PPAN-P2RY11)	NP_001035754.1:n.*93dup
NM_001198690.1:c.*977dup (PPAN-P2RY11)	NP_001185619.1:n.*977dup
NM_002566.4:c.*93dup (P2RY11)	NP_002557.2:n.*93dup
NM_002566.5:c.*93dup (P2RY11) MANE Select	NP_002557.2:n.*93dup
NM_001040664.3:c.*93dup (PPAN-P2RY11)	NP_001035754.1:n.*93dup
NM_001198690.2:c.*977dup (PPAN-P2RY11)	NP_001185619.1:n.*977dup