Canonical Allele Identifier: CA399727381
Gene: PYY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952978G>C , CM000679.2:g.43952978G>C GRCh38
NC_000017.10:g.42030346G>C , CM000679.1:g.42030346G>C GRCh37
NC_000017.9:g.39385872G>C NCBI36
NG_023338.1:g.56492C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*127C>G ENSP00000467310.1:n.*127C>G
ENST00000692052.1:c.272C>G MANE Select ENSP00000509262.1:p.Ser91Trp
ENST00000360085.6:c.272C>G ENSP00000353198.1:p.Ser91Trp
ENST00000592796.1:c.*127C>G ENSP00000467310.1:n.*127C>G
NM_004160.4:c.272C>G NP_004151.3:p.Ser91Trp
XM_011525035.1:c.272C>G XP_011523337.1:p.Ser91Trp
NM_004160.5:c.272C>G NP_004151.3:p.Ser91Trp
NM_001394028.1:c.272C>G MANE Select NP_001380957.1:p.Ser91Trp
NM_001394029.1:c.*127C>G NP_001380958.1:n.*127C>G
NM_004160.6:c.272C>G NP_004151.4:p.Ser91Trp