Canonical Allele Identifier: CA500242989

Gene: PYY

Linked Data

• MyVariant Identifiers: chr17:g.42030325C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952957C>T , CM000679.2:g.43952957C>T	GRCh38
NC_000017.10:g.42030325C>T , CM000679.1:g.42030325C>T	GRCh37
NC_000017.9:g.39385851C>T	NCBI36
NG_023338.1:g.56513G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*148G>A	ENSP00000467310.1:n.*148G>A
ENST00000692052.1:c.293G>A MANE Select	ENSP00000509262.1:p.Ter98=
ENST00000360085.6:c.293G>A	ENSP00000353198.1:p.Ter98=
ENST00000592796.1:c.*148G>A	ENSP00000467310.1:n.*148G>A
NM_004160.4:c.293G>A	NP_004151.3:p.Ter98=
XM_011525035.1:c.293G>A	XP_011523337.1:p.Ter98=
NM_004160.5:c.293G>A	NP_004151.3:p.Ter98=
NM_001394028.1:c.293G>A MANE Select	NP_001380957.1:p.Ter98=
NM_001394029.1:c.*148G>A	NP_001380958.1:n.*148G>A
NM_004160.6:c.293G>A	NP_004151.4:p.Ter98=