Canonical Allele Identifier: CA2261156712

Gene: PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952878_43952879delinsCG , CM000679.2:g.43952878_43952879delinsCG	GRCh38
NC_000017.10:g.42030246_42030247delinsCG , CM000679.1:g.42030246_42030247delinsCG	GRCh37
NC_000017.9:g.39385772_39385773delinsCG	NCBI36
NG_023338.1:g.56591_56592delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*226_*227delinsCG	ENSP00000467310.1:n.*226_*227delinsCG
ENST00000692052.1:c.*77_*78delinsCG MANE Select	ENSP00000509262.1:n.*77_*78delinsCG
ENST00000360085.6:c.*77_*78delinsCG	ENSP00000353198.1:n.*77_*78delinsCG
NM_004160.4:c.*77_*78delinsCG	NP_004151.3:n.*77_*78delinsCG
XM_011525035.1:c.*77_*78delinsCG	XP_011523337.1:n.*77_*78delinsCG
NM_004160.5:c.*77_*78delinsCG	NP_004151.3:n.*77_*78delinsCG
NM_001394028.1:c.*77_*78delinsCG MANE Select	NP_001380957.1:n.*77_*78delinsCG
NM_001394029.1:c.*226_*227delinsCG	NP_001380958.1:n.*226_*227delinsCG
NM_004160.6:c.*77_*78delinsCG	NP_004151.4:n.*77_*78delinsCG