Canonical Allele Identifier: CA2682048155

Gene: NPY

Linked Data

• gnomAD v4: 7-24285137-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285138del , CM000669.2:g.24285138del	GRCh38
NC_000007.13:g.24324757del , CM000669.1:g.24324757del	GRCh37
NC_000007.12:g.24291282del	NCBI36
NG_016148.1:g.5951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-103del MANE Select	ENSP00000242152.2:n.1-103del
ENST00000242152.6:c.1-103del	ENSP00000242152.2:n.1-103del
ENST00000405982.1:c.-103del	ENSP00000385282.1:n.-103del
ENST00000407573.5:c.-1+62del	ENSP00000384364.1:n.-1+62del
NM_000905.3:c.1-103del	NP_000896.1:n.1-103del
XM_017012910.1:c.42-29439del	XP_016868399.1:n.42-29439del
XM_017012911.1:c.42-29439del	XP_016868400.1:n.42-29439del
XR_001745121.1:n.473+34219del
XR_001745122.1:n.345-88109del
XR_001745123.1:n.473+34219del
XR_001745124.1:n.473+34219del
XR_001745125.1:n.473+34219del
XR_001745126.1:n.473+34219del
XR_001745127.1:n.345-29439del
XR_001745129.1:n.473+34219del
XR_001745130.1:n.473+34219del
XR_001745131.1:n.473+34219del
XR_001745132.1:n.473+34219del
NM_000905.4:c.1-103del MANE Select	NP_000896.1:n.1-103del