Canonical Allele Identifier: CA399727512

Gene: PYY

Linked Data

• MyVariant Identifiers: chr17:g.42030484T>C (hg19) ; chr17:g.43953116T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.262A>G	ENSP00000467310.1:p.Arg88Gly
ENST00000692052.1:c.262A>G MANE Select	ENSP00000509262.1:p.Arg88Gly
ENST00000360085.6:c.262A>G	ENSP00000353198.1:p.Arg88Gly
ENST00000592796.1:c.262A>G	ENSP00000467310.1:p.Arg88Gly
NM_004160.4:c.262A>G	NP_004151.3:p.Arg88Gly
XM_011525035.1:c.262A>G	XP_011523337.1:p.Arg88Gly
NM_004160.5:c.262A>G	NP_004151.3:p.Arg88Gly
NM_001394028.1:c.262A>G MANE Select	NP_001380957.1:p.Arg88Gly
NM_001394029.1:c.262A>G	NP_001380958.1:p.Arg88Gly
NM_004160.6:c.262A>G	NP_004151.4:p.Arg88Gly