Canonical Allele Identifier: CA2261156675

Gene: PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952837A= , CM000679.2:g.43952837A=	GRCh38
NC_000017.10:g.42030205A= , CM000679.1:g.42030205A=	GRCh37
NC_000017.9:g.39385731A=	NCBI36
NG_023338.1:g.56633T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*268T=	ENSP00000467310.1:n.*268T=
ENST00000692052.1:c.*119T= MANE Select	ENSP00000509262.1:n.*119T=
ENST00000360085.6:c.*119T=	ENSP00000353198.1:n.*119T=
NM_004160.4:c.*119T=	NP_004151.3:n.*119T=
XM_011525035.1:c.*119T=	XP_011523337.1:n.*119T=
NM_004160.5:c.*119T=	NP_004151.3:n.*119T=
NM_001394028.1:c.*119T= MANE Select	NP_001380957.1:n.*119T=
NM_001394029.1:c.*268T=	NP_001380958.1:n.*268T=
NM_004160.6:c.*119T=	NP_004151.4:n.*119T=