Canonical Allele Identifier: CA2638142943

Gene: PYY

Linked Data

• gnomAD v4: 17-43952891-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952891T>G , CM000679.2:g.43952891T>G	GRCh38
NC_000017.10:g.42030259T>G , CM000679.1:g.42030259T>G	GRCh37
NC_000017.9:g.39385785T>G	NCBI36
NG_023338.1:g.56579A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*214A>C	ENSP00000467310.1:n.*214A>C
ENST00000692052.1:c.*65A>C MANE Select	ENSP00000509262.1:n.*65A>C
ENST00000360085.6:c.*65A>C	ENSP00000353198.1:n.*65A>C
ENST00000592796.1:c.*214A>C	ENSP00000467310.1:n.*214A>C
NM_004160.4:c.*65A>C	NP_004151.3:n.*65A>C
XM_011525035.1:c.*65A>C	XP_011523337.1:n.*65A>C
NM_004160.5:c.*65A>C	NP_004151.3:n.*65A>C
NM_001394028.1:c.*65A>C MANE Select	NP_001380957.1:n.*65A>C
NM_001394029.1:c.*214A>C	NP_001380958.1:n.*214A>C
NM_004160.6:c.*65A>C	NP_004151.4:n.*65A>C