Canonical Allele Identifier: CA2682048150

Gene: NPY

Linked Data

• gnomAD v4: 7-24285135-TCGCGTGTGGTAGCAGGAGGAGGAGCGCGGGGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285137_24285169del , CM000669.2:g.24285137_24285169del	GRCh38
NC_000007.13:g.24324756_24324788del , CM000669.1:g.24324756_24324788del	GRCh37
NC_000007.12:g.24291281_24291313del	NCBI36
NG_016148.1:g.5950_5982del

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-104_1-72del MANE Select	ENSP00000242152.2:n.1-104_1-72del
ENST00000242152.6:c.1-104_1-72del	ENSP00000242152.2:n.1-104_1-72del
ENST00000405982.1:c.-104_-72del	ENSP00000385282.1:n.-104_-72del
ENST00000407573.5:c.-1+61_1-72del	ENSP00000384364.1:n.-1+61_1-72del
NM_000905.3:c.1-104_1-72del	NP_000896.1:n.1-104_1-72del
XM_017012910.1:c.42-29469_42-29437del	XP_016868399.1:n.42-29469_42-29437del
XM_017012911.1:c.42-29469_42-29437del	XP_016868400.1:n.42-29469_42-29437del
XR_001745121.1:n.473+34189_473+34221del
XR_001745122.1:n.345-88139_345-88107del
XR_001745123.1:n.473+34189_473+34221del
XR_001745124.1:n.473+34189_473+34221del
XR_001745125.1:n.473+34189_473+34221del
XR_001745126.1:n.473+34189_473+34221del
XR_001745127.1:n.345-29469_345-29437del
XR_001745129.1:n.473+34189_473+34221del
XR_001745130.1:n.473+34189_473+34221del
XR_001745131.1:n.473+34189_473+34221del
XR_001745132.1:n.473+34189_473+34221del
NM_000905.4:c.1-104_1-72del MANE Select	NP_000896.1:n.1-104_1-72del