Canonical Allele Identifier: CA645587773
Gene: PYY HGNC NCBI

Linked Data

COSMIC: COSM133410

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953112_43953113delinsTG , CM000679.2:g.43953112_43953113delinsTG GRCh38
NC_000017.10:g.42030480_42030481delinsTG , CM000679.1:g.42030480_42030481delinsTG GRCh37
NC_000017.9:g.39386006_39386007delinsTG NCBI36
NG_023338.1:g.56357_56358delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.265_266delinsCA ENSP00000467310.1:p.Ser89Gln
ENST00000692052.1:c.265_266delinsCA MANE Select ENSP00000509262.1:p.Ser89Gln
ENST00000360085.6:c.265_266delinsCA ENSP00000353198.1:p.Ser89Gln
ENST00000592796.1:c.265_266delinsCA ENSP00000467310.1:p.Ser89Gln
NM_004160.4:c.265_266delinsCA NP_004151.3:p.Ser89Gln
XM_011525035.1:c.265_266delinsCA XP_011523337.1:p.Ser89Gln
NM_004160.5:c.265_266delinsCA NP_004151.3:p.Ser89Gln
NM_001394028.1:c.265_266delinsCA MANE Select NP_001380957.1:p.Ser89Gln
NM_001394029.1:c.265_266delinsCA NP_001380958.1:p.Ser89Gln
NM_004160.6:c.265_266delinsCA NP_004151.4:p.Ser89Gln