Canonical Allele Identifier: CA2261156625
Gene: PYY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952765G= , CM000679.2:g.43952765G= GRCh38
NC_000017.10:g.42030133G= , CM000679.1:g.42030133G= GRCh37
NC_000017.9:g.39385659G= NCBI36
NG_023338.1:g.56705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*340C= ENSP00000467310.1:n.*340C=
ENST00000692052.1:c.*191C= MANE Select ENSP00000509262.1:n.*191C=
ENST00000360085.6:c.*191C= ENSP00000353198.1:n.*191C=
NM_004160.4:c.*191C= NP_004151.3:n.*191C=
XM_011525035.1:c.*191C= XP_011523337.1:n.*191C=
NM_004160.5:c.*191C= NP_004151.3:n.*191C=
NM_001394028.1:c.*191C= MANE Select NP_001380957.1:n.*191C=
NM_001394029.1:c.*340C= NP_001380958.1:n.*340C=
NM_004160.6:c.*191C= NP_004151.4:n.*191C=
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