Canonical Allele Identifier: CA772250240
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs1266729557
gnomAD v3: 17-43952971-GC-G
gnomAD v4: 17-43952971-GC-G
MyVariant Identifiers: chr17:g.42030340del (hg19) chr17:g.43952972del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952974del , CM000679.2:g.43952974del GRCh38
NC_000017.10:g.42030342del , CM000679.1:g.42030342del GRCh37
NC_000017.9:g.39385868del NCBI36
NG_023338.1:g.56498del

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*133del ENSP00000467310.1:n.*133del
ENST00000692052.1:c.278del MANE Select ENSP00000509262.1:p.Gly93AlafsTer9
ENST00000360085.6:c.278del ENSP00000353198.1:p.Gly93AlafsTer9
ENST00000592796.1:c.*133del ENSP00000467310.1:n.*133del
NM_004160.4:c.278del NP_004151.3:p.Gly93AlafsTer9
XM_011525035.1:c.278del XP_011523337.1:p.Gly93AlafsTer9
NM_004160.5:c.278del NP_004151.3:p.Gly93AlafsTer9
NM_001394028.1:c.278del MANE Select NP_001380957.1:p.Gly93AlafsTer9
NM_001394029.1:c.*133del NP_001380958.1:n.*133del
NM_004160.6:c.278del NP_004151.4:p.Gly93AlafsTer9
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