Canonical Allele Identifier: CA2638143048
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952974-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952975del , CM000679.2:g.43952975del GRCh38
NC_000017.10:g.42030343del , CM000679.1:g.42030343del GRCh37
NC_000017.9:g.39385869del NCBI36
NG_023338.1:g.56495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*130del ENSP00000467310.1:n.*130del
ENST00000692052.1:c.275del MANE Select ENSP00000509262.1:p.Glu92GlyfsTer10
ENST00000360085.6:c.275del ENSP00000353198.1:p.Glu92GlyfsTer10
ENST00000592796.1:c.*130del ENSP00000467310.1:n.*130del
NM_004160.4:c.275del NP_004151.3:p.Glu92GlyfsTer10
XM_011525035.1:c.275del XP_011523337.1:p.Glu92GlyfsTer10
NM_004160.5:c.275del NP_004151.3:p.Glu92GlyfsTer10
NM_001394028.1:c.275del MANE Select NP_001380957.1:p.Glu92GlyfsTer10
NM_001394029.1:c.*130del NP_001380958.1:n.*130del
NM_004160.6:c.275del NP_004151.4:p.Glu92GlyfsTer10
Search 100 bp 5'
Search 100 bp 3'