Canonical Allele Identifier: CA2261156821

Gene: PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953093_43953094delinsTA , CM000679.2:g.43953093_43953094delinsTA	GRCh38
NC_000017.10:g.42030461_42030462delinsTA , CM000679.1:g.42030461_42030462delinsTA	GRCh37
NC_000017.9:g.39385987_39385988delinsTA	NCBI36
NG_023338.1:g.56376_56377delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*11_*12delinsTA	ENSP00000467310.1:n.*11_*12delinsTA
ENST00000692052.1:c.269+15_269+16delinsTA MANE Select	ENSP00000509262.1:n.269+15_269+16delinsTA
ENST00000360085.6:c.269+15_269+16delinsTA	ENSP00000353198.1:n.269+15_269+16delinsTA
ENST00000592796.1:c.*11_*12delinsTA	ENSP00000467310.1:n.*11_*12delinsTA
NM_004160.4:c.269+15_269+16delinsTA	NP_004151.3:n.269+15_269+16delinsTA
XM_011525035.1:c.269+15_269+16delinsTA	XP_011523337.1:n.269+15_269+16delinsTA
NM_004160.5:c.269+15_269+16delinsTA	NP_004151.3:n.269+15_269+16delinsTA
NM_001394028.1:c.269+15_269+16delinsTA MANE Select	NP_001380957.1:n.269+15_269+16delinsTA
NM_001394029.1:c.*11_*12delinsTA	NP_001380958.1:n.*11_*12delinsTA
NM_004160.6:c.269+15_269+16delinsTA	NP_004151.4:n.269+15_269+16delinsTA