Canonical Allele Identifier: CA2638142786
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952810-G-GAAGGGAAGAGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952810_43952811insAAGGGAAGAGC , CM000679.2:g.43952810_43952811insAAGGGAAGAGC GRCh38
NC_000017.10:g.42030178_42030179insAAGGGAAGAGC , CM000679.1:g.42030178_42030179insAAGGGAAGAGC GRCh37
NC_000017.9:g.39385704_39385705insAAGGGAAGAGC NCBI36
NG_023338.1:g.56659_56660insGCTCTTCCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000592796.2:c.*294_*295insGCTCTTCCCTT ENSP00000467310.1:n.*294_*295insGCTCTTCCCTT
ENST00000692052.1:c.*145_*146insGCTCTTCCCTT MANE Select ENSP00000509262.1:n.*145_*146insGCTCTTCCCTT
ENST00000360085.6:c.*145_*146insGCTCTTCCCTT ENSP00000353198.1:n.*145_*146insGCTCTTCCCTT
NM_004160.4:c.*145_*146insGCTCTTCCCTT NP_004151.3:n.*145_*146insGCTCTTCCCTT
XM_011525035.1:c.*145_*146insGCTCTTCCCTT XP_011523337.1:n.*145_*146insGCTCTTCCCTT
NM_004160.5:c.*145_*146insGCTCTTCCCTT NP_004151.3:n.*145_*146insGCTCTTCCCTT
NM_001394028.1:c.*145_*146insGCTCTTCCCTT MANE Select NP_001380957.1:n.*145_*146insGCTCTTCCCTT
NM_001394029.1:c.*294_*295insGCTCTTCCCTT NP_001380958.1:n.*294_*295insGCTCTTCCCTT
NM_004160.6:c.*145_*146insGCTCTTCCCTT NP_004151.4:n.*145_*146insGCTCTTCCCTT
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