Canonical Allele Identifier: CA2638143096

Gene: PYY

Linked Data

• gnomAD v4: 17-43953072-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953072T>C , CM000679.2:g.43953072T>C	GRCh38
NC_000017.10:g.42030440T>C , CM000679.1:g.42030440T>C	GRCh37
NC_000017.9:g.39385966T>C	NCBI36
NG_023338.1:g.56398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*33A>G	ENSP00000467310.1:n.*33A>G
ENST00000692052.1:c.269+37A>G MANE Select	ENSP00000509262.1:n.269+37A>G
ENST00000360085.6:c.269+37A>G	ENSP00000353198.1:n.269+37A>G
ENST00000592796.1:c.*33A>G	ENSP00000467310.1:n.*33A>G
NM_004160.4:c.269+37A>G	NP_004151.3:n.269+37A>G
XM_011525035.1:c.269+37A>G	XP_011523337.1:n.269+37A>G
NM_004160.5:c.269+37A>G	NP_004151.3:n.269+37A>G
NM_001394028.1:c.269+37A>G MANE Select	NP_001380957.1:n.269+37A>G
NM_001394029.1:c.*33A>G	NP_001380958.1:n.*33A>G
NM_004160.6:c.269+37A>G	NP_004151.4:n.269+37A>G