Canonical Allele Identifier: CA2638142849

Gene: PYY

Linked Data

• gnomAD v4: 17-43952837-ACCCGAACCCTGCCCAGACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952840_43952858del , CM000679.2:g.43952840_43952858del	GRCh38
NC_000017.10:g.42030208_42030226del , CM000679.1:g.42030208_42030226del	GRCh37
NC_000017.9:g.39385734_39385752del	NCBI36
NG_023338.1:g.56614_56632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*249_*267del	ENSP00000467310.1:n.*249_*267del
ENST00000692052.1:c.*100_*118del MANE Select	ENSP00000509262.1:n.*100_*118del
ENST00000360085.6:c.*100_*118del	ENSP00000353198.1:n.*100_*118del
NM_004160.4:c.*100_*118del	NP_004151.3:n.*100_*118del
XM_011525035.1:c.*100_*118del	XP_011523337.1:n.*100_*118del
NM_004160.5:c.*100_*118del	NP_004151.3:n.*100_*118del
NM_001394028.1:c.*100_*118del MANE Select	NP_001380957.1:n.*100_*118del
NM_001394029.1:c.*249_*267del	NP_001380958.1:n.*249_*267del
NM_004160.6:c.*100_*118del	NP_004151.4:n.*100_*118del