Canonical Allele Identifier: CA2638143066
Gene: PYY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953012_43953024dup , CM000679.2:g.43953012_43953024dup GRCh38
NC_000017.10:g.42030380_42030392dup , CM000679.1:g.42030380_42030392dup GRCh37
NC_000017.9:g.39385906_39385918dup NCBI36
NG_023338.1:g.56446_56458dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*81_*93dup ENSP00000467310.1:n.*81_*93dup
ENST00000692052.1:c.270-44_270-32dup MANE Select ENSP00000509262.1:n.270-44_270-32dup
ENST00000360085.6:c.270-44_270-32dup ENSP00000353198.1:n.270-44_270-32dup
ENST00000592796.1:c.*81_*93dup ENSP00000467310.1:n.*81_*93dup
NM_004160.4:c.270-44_270-32dup NP_004151.3:n.270-44_270-32dup
XM_011525035.1:c.270-44_270-32dup XP_011523337.1:n.270-44_270-32dup
NM_004160.5:c.270-44_270-32dup NP_004151.3:n.270-44_270-32dup
NM_001394028.1:c.270-44_270-32dup MANE Select NP_001380957.1:n.270-44_270-32dup
NM_001394029.1:c.*81_*93dup NP_001380958.1:n.*81_*93dup
NM_004160.6:c.270-44_270-32dup NP_004151.4:n.270-44_270-32dup