Canonical Allele Identifier: CA2261156724
Gene: PYY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952895G= , CM000679.2:g.43952895G= GRCh38
NC_000017.10:g.42030263G= , CM000679.1:g.42030263G= GRCh37
NC_000017.9:g.39385789G= NCBI36
NG_023338.1:g.56575C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*210C= ENSP00000467310.1:n.*210C=
ENST00000692052.1:c.*61C= MANE Select ENSP00000509262.1:n.*61C=
ENST00000360085.6:c.*61C= ENSP00000353198.1:n.*61C=
ENST00000592796.1:c.*210C= ENSP00000467310.1:n.*210C=
NM_004160.4:c.*61C= NP_004151.3:n.*61C=
XM_011525035.1:c.*61C= XP_011523337.1:n.*61C=
NM_004160.5:c.*61C= NP_004151.3:n.*61C=
NM_001394028.1:c.*61C= MANE Select NP_001380957.1:n.*61C=
NM_001394029.1:c.*210C= NP_001380958.1:n.*210C=
NM_004160.6:c.*61C= NP_004151.4:n.*61C=