Canonical Allele Identifier: CA399727496
Gene: PYY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953114C>A , CM000679.2:g.43953114C>A GRCh38
NC_000017.10:g.42030482C>A , CM000679.1:g.42030482C>A GRCh37
NC_000017.9:g.39386008C>A NCBI36
NG_023338.1:g.56356G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.264G>T ENSP00000467310.1:p.Arg88Ser
ENST00000692052.1:c.264G>T MANE Select ENSP00000509262.1:p.Arg88Ser
ENST00000360085.6:c.264G>T ENSP00000353198.1:p.Arg88Ser
ENST00000592796.1:c.264G>T ENSP00000467310.1:p.Arg88Ser
NM_004160.4:c.264G>T NP_004151.3:p.Arg88Ser
XM_011525035.1:c.264G>T XP_011523337.1:p.Arg88Ser
NM_004160.5:c.264G>T NP_004151.3:p.Arg88Ser
NM_001394028.1:c.264G>T MANE Select NP_001380957.1:p.Arg88Ser
NM_001394029.1:c.264G>T NP_001380958.1:p.Arg88Ser
NM_004160.6:c.264G>T NP_004151.4:p.Arg88Ser