Canonical Allele Identifier: CA2638143141

Gene: PYY

Linked Data

• gnomAD v4: 17-43953108-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953111_43953112dup , CM000679.2:g.43953111_43953112dup	GRCh38
NC_000017.10:g.42030479_42030480dup , CM000679.1:g.42030479_42030480dup	GRCh37
NC_000017.9:g.39386005_39386006dup	NCBI36
NG_023338.1:g.56360_56361dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.268_269dup	ENSP00000467310.1:p.Ter91GlyextTer?
ENST00000692052.1:c.268_269dup MANE Select	ENSP00000509262.1:p.Ser91GlyfsTer12
ENST00000360085.6:c.268_269dup	ENSP00000353198.1:p.Ser91GlyfsTer12
ENST00000592796.1:c.268_269dup	ENSP00000467310.1:p.Ter91GlyextTer?
NM_004160.4:c.268_269dup	NP_004151.3:p.Ser91GlyfsTer12
XM_011525035.1:c.268_269dup	XP_011523337.1:p.Ser91GlyfsTer12
NM_004160.5:c.268_269dup	NP_004151.3:p.Ser91GlyfsTer12
NM_001394028.1:c.268_269dup MANE Select	NP_001380957.1:p.Ser91GlyfsTer12
NM_001394029.1:c.268_269dup	NP_001380958.1:p.Ter91GlyextTer?
NM_004160.6:c.268_269dup	NP_004151.4:p.Ser91GlyfsTer12