Canonical Allele Identifier: CA983959842

Gene: PYY

Linked Data

• dbSNP Id: rs2048641502
• gnomAD v3: 17-43952948-A-AG
• gnomAD v4: 17-43952948-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952952dup , CM000679.2:g.43952952dup	GRCh38
NC_000017.10:g.42030320dup , CM000679.1:g.42030320dup	GRCh37
NC_000017.9:g.39385846dup	NCBI36
NG_023338.1:g.56521dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*156dup	ENSP00000467310.1:n.*156dup
ENST00000692052.1:c.*7dup MANE Select	ENSP00000509262.1:n.*7dup
ENST00000360085.6:c.*7dup	ENSP00000353198.1:n.*7dup
ENST00000592796.1:c.*156dup	ENSP00000467310.1:n.*156dup
NM_004160.4:c.*7dup	NP_004151.3:n.*7dup
XM_011525035.1:c.*7dup	XP_011523337.1:n.*7dup
NM_004160.5:c.*7dup	NP_004151.3:n.*7dup
NM_001394028.1:c.*7dup MANE Select	NP_001380957.1:n.*7dup
NM_001394029.1:c.*156dup	NP_001380958.1:n.*156dup
NM_004160.6:c.*7dup	NP_004151.4:n.*7dup