Canonical Allele Identifier: CA1099400753

Gene: NPY

Linked Data

• dbSNP Id: rs1787570923
• gnomAD v3: 7-24290769-AATAATAATTATT-A
• gnomAD v4: 7-24290769-AATAATAATTATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290772_24290783del , CM000669.2:g.24290772_24290783del	GRCh38
NC_000007.13:g.24330391_24330402del , CM000669.1:g.24330391_24330402del	GRCh37
NC_000007.12:g.24296916_24296927del	NCBI36
NG_016148.1:g.11585_11596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-891_270-880del MANE Select	ENSP00000242152.2:n.270-891_270-880del
ENST00000242152.6:c.270-891_270-880del	ENSP00000242152.2:n.270-891_270-880del
ENST00000405982.1:c.270-891_270-880del	ENSP00000385282.1:n.270-891_270-880del
ENST00000407573.5:c.270-891_270-880del	ENSP00000384364.1:n.270-891_270-880del
NM_000905.3:c.270-891_270-880del	NP_000896.1:n.270-891_270-880del
XM_017012910.1:c.41+28576_41+28587del	XP_016868399.1:n.41+28576_41+28587del
XM_017012911.1:c.41+28576_41+28587del	XP_016868400.1:n.41+28576_41+28587del
XR_001745121.1:n.473+28576_473+28587del
XR_001745122.1:n.345-93752_345-93741del
XR_001745123.1:n.473+28576_473+28587del
XR_001745124.1:n.473+28576_473+28587del
XR_001745125.1:n.473+28576_473+28587del
XR_001745126.1:n.473+28576_473+28587del
XR_001745127.1:n.345-35082_345-35071del
XR_001745129.1:n.473+28576_473+28587del
XR_001745130.1:n.473+28576_473+28587del
XR_001745131.1:n.473+28576_473+28587del
XR_001745132.1:n.473+28576_473+28587del
NM_000905.4:c.270-891_270-880del MANE Select	NP_000896.1:n.270-891_270-880del