Canonical Allele Identifier: CA8594944

Gene: PYY

Linked Data

• dbSNP Id: rs781649398
• ExAC: 17:42030436 G / GATGT
• gnomAD v4: 17-43953068-G-GATGT
• MyVariant Identifiers: chr17:g.42030436_42030437insATGT (hg19) ; chr17:g.43953068_43953069insATGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953068_43953069insATGT , CM000679.2:g.43953068_43953069insATGT	GRCh38
NC_000017.10:g.42030436_42030437insATGT , CM000679.1:g.42030436_42030437insATGT	GRCh37
NC_000017.9:g.39385962_39385963insATGT	NCBI36
NG_023338.1:g.56401_56402insACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*36_*37insACAT	ENSP00000467310.1:n.*36_*37insACAT
ENST00000692052.1:c.269+40_269+41insACAT MANE Select	ENSP00000509262.1:n.269+40_269+41insACAT
ENST00000360085.6:c.269+40_269+41insACAT	ENSP00000353198.1:n.269+40_269+41insACAT
ENST00000592796.1:c.*36_*37insACAT	ENSP00000467310.1:n.*36_*37insACAT
NM_004160.4:c.269+40_269+41insACAT	NP_004151.3:n.269+40_269+41insACAT
XM_011525035.1:c.269+40_269+41insACAT	XP_011523337.1:n.269+40_269+41insACAT
NM_004160.5:c.269+40_269+41insACAT	NP_004151.3:n.269+40_269+41insACAT
NM_001394028.1:c.269+40_269+41insACAT MANE Select	NP_001380957.1:n.269+40_269+41insACAT
NM_001394029.1:c.*36_*37insACAT	NP_001380958.1:n.*36_*37insACAT
NM_004160.6:c.269+40_269+41insACAT	NP_004151.4:n.269+40_269+41insACAT