Canonical Allele Identifier: CA155829695

Gene: NPY

Linked Data

• dbSNP Id: rs747171869
• gnomAD v2: 7-24330378-A-AAATAATAAT
• gnomAD v3: 7-24290759-A-AAATAATAAT
• gnomAD v4: 7-24290759-A-AAATAATAAT
• MyVariant Identifiers: chr7:g.24330381_24330382insAATAATAAT (hg19) ; chr7:g.24330378_24330379insAATAATAAT (hg19) ; chr7:g.24290762_24290763insAATAATAAT (hg38) ; chr7:g.24290759_24290760insAATAATAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290769_24290777dup , CM000669.2:g.24290769_24290777dup	GRCh38
NC_000007.13:g.24330388_24330396dup , CM000669.1:g.24330388_24330396dup	GRCh37
NC_000007.12:g.24296913_24296921dup	NCBI36
NG_016148.1:g.11582_11590dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-894_270-886dup MANE Select	ENSP00000242152.2:n.270-894_270-886dup
ENST00000242152.6:c.270-894_270-886dup	ENSP00000242152.2:n.270-894_270-886dup
ENST00000405982.1:c.270-894_270-886dup	ENSP00000385282.1:n.270-894_270-886dup
ENST00000407573.5:c.270-894_270-886dup	ENSP00000384364.1:n.270-894_270-886dup
NM_000905.3:c.270-894_270-886dup	NP_000896.1:n.270-894_270-886dup
XM_017012910.1:c.41+28589_41+28597dup	XP_016868399.1:n.41+28589_41+28597dup
XM_017012911.1:c.41+28589_41+28597dup	XP_016868400.1:n.41+28589_41+28597dup
XR_001745121.1:n.473+28589_473+28597dup
XR_001745122.1:n.345-93739_345-93731dup
XR_001745123.1:n.473+28589_473+28597dup
XR_001745124.1:n.473+28589_473+28597dup
XR_001745125.1:n.473+28589_473+28597dup
XR_001745126.1:n.473+28589_473+28597dup
XR_001745127.1:n.345-35069_345-35061dup
XR_001745129.1:n.473+28589_473+28597dup
XR_001745130.1:n.473+28589_473+28597dup
XR_001745131.1:n.473+28589_473+28597dup
XR_001745132.1:n.473+28589_473+28597dup
NM_000905.4:c.270-894_270-886dup MANE Select	NP_000896.1:n.270-894_270-886dup