Canonical Allele Identifier: CA399727339

Gene: PYY

Linked Data

• gnomAD v4: 17-43952972-C-A
• MyVariant Identifiers: chr17:g.42030340C>A (hg19) ; chr17:g.43952972C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952972C>A , CM000679.2:g.43952972C>A	GRCh38
NC_000017.10:g.42030340C>A , CM000679.1:g.42030340C>A	GRCh37
NC_000017.9:g.39385866C>A	NCBI36
NG_023338.1:g.56498G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*133G>T	ENSP00000467310.1:n.*133G>T
ENST00000692052.1:c.278G>T MANE Select	ENSP00000509262.1:p.Gly93Val
ENST00000360085.6:c.278G>T	ENSP00000353198.1:p.Gly93Val
ENST00000592796.1:c.*133G>T	ENSP00000467310.1:n.*133G>T
NM_004160.4:c.278G>T	NP_004151.3:p.Gly93Val
XM_011525035.1:c.278G>T	XP_011523337.1:p.Gly93Val
NM_004160.5:c.278G>T	NP_004151.3:p.Gly93Val
NM_001394028.1:c.278G>T MANE Select	NP_001380957.1:p.Gly93Val
NM_001394029.1:c.*133G>T	NP_001380958.1:n.*133G>T
NM_004160.6:c.278G>T	NP_004151.4:p.Gly93Val