Canonical Allele Identifier: CA454131810

Gene: NPY

Linked Data

• gnomAD v4: 7-24285246-A-G
• COSMIC: COSM485223
• MyVariant Identifiers: chr7:g.24324865A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285246A>G , CM000669.2:g.24285246A>G	GRCh38
NC_000007.13:g.24324865A>G , CM000669.1:g.24324865A>G	GRCh37
NC_000007.12:g.24291390A>G	NCBI36
NG_016148.1:g.6059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.6A>G MANE Select	ENSP00000242152.2:p.Leu2=
ENST00000242152.6:c.6A>G	ENSP00000242152.2:p.Leu2=
ENST00000405982.1:c.6A>G	ENSP00000385282.1:p.Leu2=
ENST00000407573.5:c.6A>G	ENSP00000384364.1:p.Leu2=
NM_000905.3:c.6A>G	NP_000896.1:p.Leu2=
XM_017012910.1:c.42-29547T>C	XP_016868399.1:n.42-29547T>C
XM_017012911.1:c.42-29547T>C	XP_016868400.1:n.42-29547T>C
XR_001745121.1:n.473+34111T>C
XR_001745122.1:n.345-88217T>C
XR_001745123.1:n.473+34111T>C
XR_001745124.1:n.473+34111T>C
XR_001745125.1:n.473+34111T>C
XR_001745126.1:n.473+34111T>C
XR_001745127.1:n.345-29547T>C
XR_001745129.1:n.473+34111T>C
XR_001745130.1:n.473+34111T>C
XR_001745131.1:n.473+34111T>C
XR_001745132.1:n.473+34111T>C
NM_000905.4:c.6A>G MANE Select	NP_000896.1:p.Leu2=