Canonical Allele Identifier: CA1099401397

Gene: NPY

Linked Data

• dbSNP Id: rs1787623702
• gnomAD v3: 7-24291734-A-AT
• gnomAD v4: 7-24291734-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291737dup , CM000669.2:g.24291737dup	GRCh38
NC_000007.13:g.24331356dup , CM000669.1:g.24331356dup	GRCh37
NC_000007.12:g.24297881dup	NCBI36
NG_016148.1:g.12550dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*50dup MANE Select	ENSP00000242152.2:n.*50dup
ENST00000242152.6:c.*50dup	ENSP00000242152.2:n.*50dup
ENST00000405982.1:c.*50dup	ENSP00000385282.1:n.*50dup
ENST00000407573.5:c.*50dup	ENSP00000384364.1:n.*50dup
NM_000905.3:c.*50dup	NP_000896.1:n.*50dup
XM_017012910.1:c.41+27622dup	XP_016868399.1:n.41+27622dup
XM_017012911.1:c.41+27622dup	XP_016868400.1:n.41+27622dup
XR_001745121.1:n.473+27622dup
XR_001745122.1:n.345-94706dup
XR_001745123.1:n.473+27622dup
XR_001745124.1:n.473+27622dup
XR_001745125.1:n.473+27622dup
XR_001745126.1:n.473+27622dup
XR_001745127.1:n.345-36036dup
XR_001745129.1:n.473+27622dup
XR_001745130.1:n.473+27622dup
XR_001745131.1:n.473+27622dup
XR_001745132.1:n.473+27622dup
NM_000905.4:c.*50dup MANE Select	NP_000896.1:n.*50dup