Canonical Allele Identifier: CA772250208

Gene: PYY

Linked Data

• dbSNP Id: rs1439403520
• MyVariant Identifiers: chr17:g.42030309A>T (hg19) ; chr17:g.43952941A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952941A>T , CM000679.2:g.43952941A>T	GRCh38
NC_000017.10:g.42030309A>T , CM000679.1:g.42030309A>T	GRCh37
NC_000017.9:g.39385835A>T	NCBI36
NG_023338.1:g.56529T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*164T>A	ENSP00000467310.1:n.*164T>A
ENST00000692052.1:c.*15T>A MANE Select	ENSP00000509262.1:n.*15T>A
ENST00000360085.6:c.*15T>A	ENSP00000353198.1:n.*15T>A
ENST00000592796.1:c.*164T>A	ENSP00000467310.1:n.*164T>A
NM_004160.4:c.*15T>A	NP_004151.3:n.*15T>A
XM_011525035.1:c.*15T>A	XP_011523337.1:n.*15T>A
NM_004160.5:c.*15T>A	NP_004151.3:n.*15T>A
NM_001394028.1:c.*15T>A MANE Select	NP_001380957.1:n.*15T>A
NM_001394029.1:c.*164T>A	NP_001380958.1:n.*164T>A
NM_004160.6:c.*15T>A	NP_004151.4:n.*15T>A