Canonical Allele Identifier: CA2261156664

Gene: PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952820_43952831delinsCGCGGGCGGAGG , CM000679.2:g.43952820_43952831delinsCGCGGGCGGAGG	GRCh38
NC_000017.10:g.42030188_42030199delinsCGCGGGCGGAGG , CM000679.1:g.42030188_42030199delinsCGCGGGCGGAGG	GRCh37
NC_000017.9:g.39385714_39385725delinsCGCGGGCGGAGG	NCBI36
NG_023338.1:g.56639_56650delinsCCTCCGCCCGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*274_*285delinsCCTCCGCCCGCG	ENSP00000467310.1:n.*274_*285delinsCCTCCGCCCGCG
ENST00000692052.1:c.*125_*136delinsCCTCCGCCCGCG MANE Select	ENSP00000509262.1:n.*125_*136delinsCCTCCGCCCGCG
ENST00000360085.6:c.*125_*136delinsCCTCCGCCCGCG	ENSP00000353198.1:n.*125_*136delinsCCTCCGCCCGCG
NM_004160.4:c.*125_*136delinsCCTCCGCCCGCG	NP_004151.3:n.*125_*136delinsCCTCCGCCCGCG
XM_011525035.1:c.*125_*136delinsCCTCCGCCCGCG	XP_011523337.1:n.*125_*136delinsCCTCCGCCCGCG
NM_004160.5:c.*125_*136delinsCCTCCGCCCGCG	NP_004151.3:n.*125_*136delinsCCTCCGCCCGCG
NM_001394028.1:c.*125_*136delinsCCTCCGCCCGCG MANE Select	NP_001380957.1:n.*125_*136delinsCCTCCGCCCGCG
NM_001394029.1:c.*274_*285delinsCCTCCGCCCGCG	NP_001380958.1:n.*274_*285delinsCCTCCGCCCGCG
NM_004160.6:c.*125_*136delinsCCTCCGCCCGCG	NP_004151.4:n.*125_*136delinsCCTCCGCCCGCG