Canonical Allele Identifier: CA399727335
Gene: PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42030338G>T (hg19) chr17:g.43952970G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952970G>T , CM000679.2:g.43952970G>T GRCh38
NC_000017.10:g.42030338G>T , CM000679.1:g.42030338G>T GRCh37
NC_000017.9:g.39385864G>T NCBI36
NG_023338.1:g.56500C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*135C>A ENSP00000467310.1:n.*135C>A
ENST00000692052.1:c.280C>A MANE Select ENSP00000509262.1:p.Pro94Thr
ENST00000360085.6:c.280C>A ENSP00000353198.1:p.Pro94Thr
ENST00000592796.1:c.*135C>A ENSP00000467310.1:n.*135C>A
NM_004160.4:c.280C>A NP_004151.3:p.Pro94Thr
XM_011525035.1:c.280C>A XP_011523337.1:p.Pro94Thr
NM_004160.5:c.280C>A NP_004151.3:p.Pro94Thr
NM_001394028.1:c.280C>A MANE Select NP_001380957.1:p.Pro94Thr
NM_001394029.1:c.*135C>A NP_001380958.1:n.*135C>A
NM_004160.6:c.280C>A NP_004151.4:p.Pro94Thr
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