Canonical Allele Identifier: CA2638142792
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952813-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952813A>T , CM000679.2:g.43952813A>T GRCh38
NC_000017.10:g.42030181A>T , CM000679.1:g.42030181A>T GRCh37
NC_000017.9:g.39385707A>T NCBI36
NG_023338.1:g.56657T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000592796.2:c.*292T>A ENSP00000467310.1:n.*292T>A
ENST00000692052.1:c.*143T>A MANE Select ENSP00000509262.1:n.*143T>A
ENST00000360085.6:c.*143T>A ENSP00000353198.1:n.*143T>A
NM_004160.4:c.*143T>A NP_004151.3:n.*143T>A
XM_011525035.1:c.*143T>A XP_011523337.1:n.*143T>A
NM_004160.5:c.*143T>A NP_004151.3:n.*143T>A
NM_001394028.1:c.*143T>A MANE Select NP_001380957.1:n.*143T>A
NM_001394029.1:c.*292T>A NP_001380958.1:n.*292T>A
NM_004160.6:c.*143T>A NP_004151.4:n.*143T>A
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