Canonical Allele Identifier: CA399727385

Gene: PYY

Linked Data

• dbSNP Id: rs1224926082
• MyVariant Identifiers: chr17:g.42030347A>C (hg19) ; chr17:g.43952979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952979A>C , CM000679.2:g.43952979A>C	GRCh38
NC_000017.10:g.42030347A>C , CM000679.1:g.42030347A>C	GRCh37
NC_000017.9:g.39385873A>C	NCBI36
NG_023338.1:g.56491T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*126T>G	ENSP00000467310.1:n.*126T>G
ENST00000692052.1:c.271T>G MANE Select	ENSP00000509262.1:p.Ser91Ala
ENST00000360085.6:c.271T>G	ENSP00000353198.1:p.Ser91Ala
ENST00000592796.1:c.*126T>G	ENSP00000467310.1:n.*126T>G
NM_004160.4:c.271T>G	NP_004151.3:p.Ser91Ala
XM_011525035.1:c.271T>G	XP_011523337.1:p.Ser91Ala
NM_004160.5:c.271T>G	NP_004151.3:p.Ser91Ala
NM_001394028.1:c.271T>G MANE Select	NP_001380957.1:p.Ser91Ala
NM_001394029.1:c.*126T>G	NP_001380958.1:n.*126T>G
NM_004160.6:c.271T>G	NP_004151.4:p.Ser91Ala