Canonical Allele Identifier: CA2638143051

Gene: PYY

Linked Data

• gnomAD v4: 17-43952984-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952986del , CM000679.2:g.43952986del	GRCh38
NC_000017.10:g.42030354del , CM000679.1:g.42030354del	GRCh37
NC_000017.9:g.39385880del	NCBI36
NG_023338.1:g.56485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*120del	ENSP00000467310.1:n.*120del
ENST00000692052.1:c.270-5del MANE Select	ENSP00000509262.1:n.270-5del
ENST00000360085.6:c.270-5del	ENSP00000353198.1:n.270-5del
ENST00000592796.1:c.*120del	ENSP00000467310.1:n.*120del
NM_004160.4:c.270-5del	NP_004151.3:n.270-5del
XM_011525035.1:c.270-5del	XP_011523337.1:n.270-5del
NM_004160.5:c.270-5del	NP_004151.3:n.270-5del
NM_001394028.1:c.270-5del MANE Select	NP_001380957.1:n.270-5del
NM_001394029.1:c.*120del	NP_001380958.1:n.*120del
NM_004160.6:c.270-5del	NP_004151.4:n.270-5del