Canonical Allele Identifier: CA155829086

Gene: NPY

Linked Data

• ClinVar Variation Id: 1900667
• ClinVar RCV Id: RCV002585809
• dbSNP Id: rs961184030
• gnomAD v3: 7-24285271-G-A
• gnomAD v4: 7-24285271-G-A
• MyVariant Identifiers: chr7:g.24324890G>A (hg19) ; chr7:g.24285271G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285271G>A , CM000669.2:g.24285271G>A	GRCh38
NC_000007.13:g.24324890G>A , CM000669.1:g.24324890G>A	GRCh37
NC_000007.12:g.24291415G>A	NCBI36
NG_016148.1:g.6084G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.31G>A MANE Select	ENSP00000242152.2:p.Gly11Arg
ENST00000242152.6:c.31G>A	ENSP00000242152.2:p.Gly11Arg
ENST00000405982.1:c.31G>A	ENSP00000385282.1:p.Gly11Arg
ENST00000407573.5:c.31G>A	ENSP00000384364.1:p.Gly11Arg
NM_000905.3:c.31G>A	NP_000896.1:p.Gly11Arg
XM_017012910.1:c.42-29572C>T	XP_016868399.1:n.42-29572C>T
XM_017012911.1:c.42-29572C>T	XP_016868400.1:n.42-29572C>T
XR_001745121.1:n.473+34086C>T
XR_001745122.1:n.345-88242C>T
XR_001745123.1:n.473+34086C>T
XR_001745124.1:n.473+34086C>T
XR_001745125.1:n.473+34086C>T
XR_001745126.1:n.473+34086C>T
XR_001745127.1:n.345-29572C>T
XR_001745129.1:n.473+34086C>T
XR_001745130.1:n.473+34086C>T
XR_001745131.1:n.473+34086C>T
XR_001745132.1:n.473+34086C>T
NM_000905.4:c.31G>A MANE Select	NP_000896.1:p.Gly11Arg