Canonical Allele Identifier: CA2638143053

Gene: PYY

Linked Data

• gnomAD v4: 17-43952990-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952990C>A , CM000679.2:g.43952990C>A	GRCh38
NC_000017.10:g.42030358C>A , CM000679.1:g.42030358C>A	GRCh37
NC_000017.9:g.39385884C>A	NCBI36
NG_023338.1:g.56480G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*115G>T	ENSP00000467310.1:n.*115G>T
ENST00000692052.1:c.270-10G>T MANE Select	ENSP00000509262.1:n.270-10G>T
ENST00000360085.6:c.270-10G>T	ENSP00000353198.1:n.270-10G>T
ENST00000592796.1:c.*115G>T	ENSP00000467310.1:n.*115G>T
NM_004160.4:c.270-10G>T	NP_004151.3:n.270-10G>T
XM_011525035.1:c.270-10G>T	XP_011523337.1:n.270-10G>T
NM_004160.5:c.270-10G>T	NP_004151.3:n.270-10G>T
NM_001394028.1:c.270-10G>T MANE Select	NP_001380957.1:n.270-10G>T
NM_001394029.1:c.*115G>T	NP_001380958.1:n.*115G>T
NM_004160.6:c.270-10G>T	NP_004151.4:n.270-10G>T