Canonical Allele Identifier: CA500612457

Gene: PYY

Linked Data

• MyVariant Identifiers: chr17:g.42030484T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953116T>G , CM000679.2:g.43953116T>G	GRCh38
NC_000017.10:g.42030484T>G , CM000679.1:g.42030484T>G	GRCh37
NC_000017.9:g.39386010T>G	NCBI36
NG_023338.1:g.56354A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.262A>C	ENSP00000467310.1:p.Arg88=
ENST00000692052.1:c.262A>C MANE Select	ENSP00000509262.1:p.Arg88=
ENST00000360085.6:c.262A>C	ENSP00000353198.1:p.Arg88=
ENST00000592796.1:c.262A>C	ENSP00000467310.1:p.Arg88=
NM_004160.4:c.262A>C	NP_004151.3:p.Arg88=
XM_011525035.1:c.262A>C	XP_011523337.1:p.Arg88=
NM_004160.5:c.262A>C	NP_004151.3:p.Arg88=
NM_001394028.1:c.262A>C MANE Select	NP_001380957.1:p.Arg88=
NM_001394029.1:c.262A>C	NP_001380958.1:p.Arg88=
NM_004160.6:c.262A>C	NP_004151.4:p.Arg88=