Canonical Allele Identifier: CA399727244

Gene: PYY

Linked Data

• gnomAD v4: 17-43952958-A-G
• MyVariant Identifiers: chr17:g.42030326A>G (hg19) ; chr17:g.43952958A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952958A>G , CM000679.2:g.43952958A>G	GRCh38
NC_000017.10:g.42030326A>G , CM000679.1:g.42030326A>G	GRCh37
NC_000017.9:g.39385852A>G	NCBI36
NG_023338.1:g.56512T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*147T>C	ENSP00000467310.1:n.*147T>C
ENST00000692052.1:c.292T>C MANE Select	ENSP00000509262.1:p.Ter98Arg
ENST00000360085.6:c.292T>C	ENSP00000353198.1:p.Ter98Arg
ENST00000592796.1:c.*147T>C	ENSP00000467310.1:n.*147T>C
NM_004160.4:c.292T>C	NP_004151.3:p.Ter98Arg
XM_011525035.1:c.292T>C	XP_011523337.1:p.Ter98Arg
NM_004160.5:c.292T>C	NP_004151.3:p.Ter98Arg
NM_001394028.1:c.292T>C MANE Select	NP_001380957.1:p.Ter98Arg
NM_001394029.1:c.*147T>C	NP_001380958.1:n.*147T>C
NM_004160.6:c.292T>C	NP_004151.4:p.Ter98Arg