Canonical Allele Identifier: CA399727282

Gene: PYY

Linked Data

• MyVariant Identifiers: chr17:g.42030332G>C (hg19) ; chr17:g.43952964G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952964G>C , CM000679.2:g.43952964G>C	GRCh38
NC_000017.10:g.42030332G>C , CM000679.1:g.42030332G>C	GRCh37
NC_000017.9:g.39385858G>C	NCBI36
NG_023338.1:g.56506C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*141C>G	ENSP00000467310.1:n.*141C>G
ENST00000692052.1:c.286C>G MANE Select	ENSP00000509262.1:p.Leu96Val
ENST00000360085.6:c.286C>G	ENSP00000353198.1:p.Leu96Val
ENST00000592796.1:c.*141C>G	ENSP00000467310.1:n.*141C>G
NM_004160.4:c.286C>G	NP_004151.3:p.Leu96Val
XM_011525035.1:c.286C>G	XP_011523337.1:p.Leu96Val
NM_004160.5:c.286C>G	NP_004151.3:p.Leu96Val
NM_001394028.1:c.286C>G MANE Select	NP_001380957.1:p.Leu96Val
NM_001394029.1:c.*141C>G	NP_001380958.1:n.*141C>G
NM_004160.6:c.286C>G	NP_004151.4:p.Leu96Val