Canonical Allele Identifier: CA2638142676

Gene: PYY

Linked Data

• gnomAD v4: 17-43952755-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952758del , CM000679.2:g.43952758del	GRCh38
NC_000017.10:g.42030126del , CM000679.1:g.42030126del	GRCh37
NC_000017.9:g.39385652del	NCBI36
NG_023338.1:g.56714del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*349del	ENSP00000467310.1:n.*349del
ENST00000692052.1:c.*200del MANE Select	ENSP00000509262.1:n.*200del
ENST00000360085.6:c.*200del	ENSP00000353198.1:n.*200del
NM_004160.4:c.*200del	NP_004151.3:n.*200del
XM_011525035.1:c.*200del	XP_011523337.1:n.*200del
NM_004160.5:c.*200del	NP_004151.3:n.*200del
NM_001394028.1:c.*200del MANE Select	NP_001380957.1:n.*200del
NM_001394029.1:c.*349del	NP_001380958.1:n.*349del
NM_004160.6:c.*200del	NP_004151.4:n.*200del