Canonical Allele Identifier: CA2809576022
Gene: PYY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952811_43952812del , CM000679.2:g.43952811_43952812del GRCh38
NC_000017.10:g.42030179_42030180del , CM000679.1:g.42030179_42030180del GRCh37
NC_000017.9:g.39385705_39385706del NCBI36
NG_023338.1:g.56658_56659del

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*293_*294del ENSP00000467310.1:n.*293_*294del
ENST00000692052.1:c.*144_*145del MANE Select ENSP00000509262.1:n.*144_*145del
ENST00000360085.6:c.*144_*145del ENSP00000353198.1:n.*144_*145del
NM_004160.4:c.*144_*145del NP_004151.3:n.*144_*145del
XM_011525035.1:c.*144_*145del XP_011523337.1:n.*144_*145del
NM_004160.5:c.*144_*145del NP_004151.3:n.*144_*145del
NM_001394028.1:c.*144_*145del MANE Select NP_001380957.1:n.*144_*145del
NM_001394029.1:c.*293_*294del NP_001380958.1:n.*293_*294del
NM_004160.6:c.*144_*145del NP_004151.4:n.*144_*145del