Canonical Allele Identifier: CA2638142782

Gene: PYY

Linked Data

• gnomAD v4: 17-43952809-G-GGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952810_43952811insAAG , CM000679.2:g.43952810_43952811insAAG	GRCh38
NC_000017.10:g.42030178_42030179insAAG , CM000679.1:g.42030178_42030179insAAG	GRCh37
NC_000017.9:g.39385704_39385705insAAG	NCBI36
NG_023338.1:g.56660_56661insTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000592796.2:c.*295_*296insTTC	ENSP00000467310.1:n.*295_*296insTTC
ENST00000692052.1:c.*146_*147insTTC MANE Select	ENSP00000509262.1:n.*146_*147insTTC
ENST00000360085.6:c.*146_*147insTTC	ENSP00000353198.1:n.*146_*147insTTC
NM_004160.4:c.*146_*147insTTC	NP_004151.3:n.*146_*147insTTC
XM_011525035.1:c.*146_*147insTTC	XP_011523337.1:n.*146_*147insTTC
NM_004160.5:c.*146_*147insTTC	NP_004151.3:n.*146_*147insTTC
NM_001394028.1:c.*146_*147insTTC MANE Select	NP_001380957.1:n.*146_*147insTTC
NM_001394029.1:c.*295_*296insTTC	NP_001380958.1:n.*295_*296insTTC
NM_004160.6:c.*146_*147insTTC	NP_004151.4:n.*146_*147insTTC