Canonical Allele Identifier: CA836897952

Gene: NPY

Linked Data

• dbSNP Id: rs1491371924
• MyVariant Identifiers: chr7:g.24330388_24330389del (hg19) ; chr7:g.24290769_24290770del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290769_24290770del , CM000669.2:g.24290769_24290770del	GRCh38
NC_000007.13:g.24330388_24330389del , CM000669.1:g.24330388_24330389del	GRCh37
NC_000007.12:g.24296913_24296914del	NCBI36
NG_016148.1:g.11582_11583del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-894_270-893del MANE Select	ENSP00000242152.2:n.270-894_270-893del
ENST00000242152.6:c.270-894_270-893del	ENSP00000242152.2:n.270-894_270-893del
ENST00000405982.1:c.270-894_270-893del	ENSP00000385282.1:n.270-894_270-893del
ENST00000407573.5:c.270-894_270-893del	ENSP00000384364.1:n.270-894_270-893del
NM_000905.3:c.270-894_270-893del	NP_000896.1:n.270-894_270-893del
XM_017012910.1:c.41+28587_41+28588del	XP_016868399.1:n.41+28587_41+28588del
XM_017012911.1:c.41+28587_41+28588del	XP_016868400.1:n.41+28587_41+28588del
XR_001745121.1:n.473+28587_473+28588del
XR_001745122.1:n.345-93741_345-93740del
XR_001745123.1:n.473+28587_473+28588del
XR_001745124.1:n.473+28587_473+28588del
XR_001745125.1:n.473+28587_473+28588del
XR_001745126.1:n.473+28587_473+28588del
XR_001745127.1:n.345-35071_345-35070del
XR_001745129.1:n.473+28587_473+28588del
XR_001745130.1:n.473+28587_473+28588del
XR_001745131.1:n.473+28587_473+28588del
XR_001745132.1:n.473+28587_473+28588del
NM_000905.4:c.270-894_270-893del MANE Select	NP_000896.1:n.270-894_270-893del