Canonical Allele Identifier: CA2536580795

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290744del , CM000669.2:g.24290744del	GRCh38
NC_000007.13:g.24330363del , CM000669.1:g.24330363del	GRCh37
NC_000007.12:g.24296888del	NCBI36
NG_016148.1:g.11557del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-919del MANE Select	ENSP00000242152.2:n.270-919del
ENST00000242152.6:c.270-919del	ENSP00000242152.2:n.270-919del
ENST00000405982.1:c.270-919del	ENSP00000385282.1:n.270-919del
ENST00000407573.5:c.270-919del	ENSP00000384364.1:n.270-919del
NM_000905.3:c.270-919del	NP_000896.1:n.270-919del
XM_017012910.1:c.41+28614del	XP_016868399.1:n.41+28614del
XM_017012911.1:c.41+28614del	XP_016868400.1:n.41+28614del
XR_001745121.1:n.473+28614del
XR_001745122.1:n.345-93714del
XR_001745123.1:n.473+28614del
XR_001745124.1:n.473+28614del
XR_001745125.1:n.473+28614del
XR_001745126.1:n.473+28614del
XR_001745127.1:n.345-35044del
XR_001745129.1:n.473+28614del
XR_001745130.1:n.473+28614del
XR_001745131.1:n.473+28614del
XR_001745132.1:n.473+28614del
NM_000905.4:c.270-919del MANE Select	NP_000896.1:n.270-919del