Canonical Allele Identifier: CA2638143090

Gene: PYY

Linked Data

• gnomAD v4: 17-43953063-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953063A>T , CM000679.2:g.43953063A>T	GRCh38
NC_000017.10:g.42030431A>T , CM000679.1:g.42030431A>T	GRCh37
NC_000017.9:g.39385957A>T	NCBI36
NG_023338.1:g.56407T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*42T>A	ENSP00000467310.1:n.*42T>A
ENST00000692052.1:c.269+46T>A MANE Select	ENSP00000509262.1:n.269+46T>A
ENST00000360085.6:c.269+46T>A	ENSP00000353198.1:n.269+46T>A
ENST00000592796.1:c.*42T>A	ENSP00000467310.1:n.*42T>A
NM_004160.4:c.269+46T>A	NP_004151.3:n.269+46T>A
XM_011525035.1:c.269+46T>A	XP_011523337.1:n.269+46T>A
NM_004160.5:c.269+46T>A	NP_004151.3:n.269+46T>A
NM_001394028.1:c.269+46T>A MANE Select	NP_001380957.1:n.269+46T>A
NM_001394029.1:c.*42T>A	NP_001380958.1:n.*42T>A
NM_004160.6:c.269+46T>A	NP_004151.4:n.269+46T>A