Canonical Allele Identifier: CA2261156836

Gene: PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953127T= , CM000679.2:g.43953127T=	GRCh38
NC_000017.10:g.42030495T= , CM000679.1:g.42030495T=	GRCh37
NC_000017.9:g.39386021T=	NCBI36
NG_023338.1:g.56343A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.251A=	ENSP00000467310.1:p.Asp84=
ENST00000692052.1:c.251A= MANE Select	ENSP00000509262.1:p.Asp84=
ENST00000360085.6:c.251A=	ENSP00000353198.1:p.Asp84=
ENST00000592796.1:c.251A=	ENSP00000467310.1:p.Asp84=
NM_004160.4:c.251A=	NP_004151.3:p.Asp84=
XM_011525035.1:c.251A=	XP_011523337.1:p.Asp84=
NM_004160.5:c.251A=	NP_004151.3:p.Asp84=
NM_001394028.1:c.251A= MANE Select	NP_001380957.1:p.Asp84=
NM_001394029.1:c.251A=	NP_001380958.1:p.Asp84=
NM_004160.6:c.251A=	NP_004151.4:p.Asp84=