Canonical Allele Identifier: CA2261156826

Gene: PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953108C= , CM000679.2:g.43953108C=	GRCh38
NC_000017.10:g.42030476C= , CM000679.1:g.42030476C=	GRCh37
NC_000017.9:g.39386002C=	NCBI36
NG_023338.1:g.56362G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.270G=	ENSP00000467310.1:p.Arg90=
ENST00000692052.1:c.269+1G= MANE Select	ENSP00000509262.1:n.269+1G=
ENST00000360085.6:c.269+1G=	ENSP00000353198.1:n.269+1G=
ENST00000592796.1:c.270G=	ENSP00000467310.1:p.Arg90=
NM_004160.4:c.269+1G=	NP_004151.3:n.269+1G=
XM_011525035.1:c.269+1G=	XP_011523337.1:n.269+1G=
NM_004160.5:c.269+1G=	NP_004151.3:n.269+1G=
NM_001394028.1:c.269+1G= MANE Select	NP_001380957.1:n.269+1G=
NM_001394029.1:c.270G=	NP_001380958.1:p.Arg90=
NM_004160.6:c.269+1G=	NP_004151.4:n.269+1G=