Canonical Allele Identifier: CA155829822

Gene: NPY

Linked Data

• dbSNP Id: rs369109190
• gnomAD v2: 7-24331403-A-G
• gnomAD v3: 7-24291784-A-G
• gnomAD v4: 7-24291784-A-G
• MyVariant Identifiers: chr7:g.24331403A>G (hg19) ; chr7:g.24291784A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291784A>G , CM000669.2:g.24291784A>G	GRCh38
NC_000007.13:g.24331403A>G , CM000669.1:g.24331403A>G	GRCh37
NC_000007.12:g.24297928A>G	NCBI36
NG_016148.1:g.12597A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*97A>G MANE Select	ENSP00000242152.2:n.*97A>G
ENST00000242152.6:c.*97A>G	ENSP00000242152.2:n.*97A>G
ENST00000405982.1:c.*97A>G	ENSP00000385282.1:n.*97A>G
ENST00000407573.5:c.*97A>G	ENSP00000384364.1:n.*97A>G
NM_000905.3:c.*97A>G	NP_000896.1:n.*97A>G
XM_017012910.1:c.41+27573T>C	XP_016868399.1:n.41+27573T>C
XM_017012911.1:c.41+27573T>C	XP_016868400.1:n.41+27573T>C
XR_001745121.1:n.473+27573T>C
XR_001745122.1:n.345-94755T>C
XR_001745123.1:n.473+27573T>C
XR_001745124.1:n.473+27573T>C
XR_001745125.1:n.473+27573T>C
XR_001745126.1:n.473+27573T>C
XR_001745127.1:n.345-36085T>C
XR_001745129.1:n.473+27573T>C
XR_001745130.1:n.473+27573T>C
XR_001745131.1:n.473+27573T>C
XR_001745132.1:n.473+27573T>C
NM_000905.4:c.*97A>G MANE Select	NP_000896.1:n.*97A>G