Canonical Allele Identifier: CA2261156824
Gene: PYY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953100C= , CM000679.2:g.43953100C= GRCh38
NC_000017.10:g.42030468C= , CM000679.1:g.42030468C= GRCh37
NC_000017.9:g.39385994C= NCBI36
NG_023338.1:g.56370G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*5G= ENSP00000467310.1:n.*5G=
ENST00000692052.1:c.269+9G= MANE Select ENSP00000509262.1:n.269+9G=
ENST00000360085.6:c.269+9G= ENSP00000353198.1:n.269+9G=
ENST00000592796.1:c.*5G= ENSP00000467310.1:n.*5G=
NM_004160.4:c.269+9G= NP_004151.3:n.269+9G=
XM_011525035.1:c.269+9G= XP_011523337.1:n.269+9G=
NM_004160.5:c.269+9G= NP_004151.3:n.269+9G=
NM_001394028.1:c.269+9G= MANE Select NP_001380957.1:n.269+9G=
NM_001394029.1:c.*5G= NP_001380958.1:n.*5G=
NM_004160.6:c.269+9G= NP_004151.4:n.269+9G=
Search 100 bp 5'
Search 100 bp 3'