Canonical Allele Identifier: CA2638143140

Gene: PYY

Linked Data

• gnomAD v4: 17-43953108-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953111_43953112del , CM000679.2:g.43953111_43953112del	GRCh38
NC_000017.10:g.42030479_42030480del , CM000679.1:g.42030479_42030480del	GRCh37
NC_000017.9:g.39386005_39386006del	NCBI36
NG_023338.1:g.56360_56361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.268_269del	ENSP00000467310.1:p.Arg90ValfsTer24
ENST00000692052.1:c.268_269del MANE Select	ENSP00000509262.1:p.Arg90ValfsTer?
ENST00000360085.6:c.268_269del	ENSP00000353198.1:p.Arg90ValfsTer?
ENST00000592796.1:c.268_269del	ENSP00000467310.1:p.Arg90ValfsTer24
NM_004160.4:c.268_269del	NP_004151.3:p.Arg90ValfsTer?
XM_011525035.1:c.268_269del	XP_011523337.1:p.Arg90ValfsTer?
NM_004160.5:c.268_269del	NP_004151.3:p.Arg90ValfsTer?
NM_001394028.1:c.268_269del MANE Select	NP_001380957.1:p.Arg90ValfsTer?
NM_001394029.1:c.268_269del	NP_001380958.1:p.Arg90ValfsTer24
NM_004160.6:c.268_269del	NP_004151.4:p.Arg90ValfsTer?