Canonical Allele Identifier: CA2682048157

Gene: NPY

Linked Data

• gnomAD v4: 7-24285138-C-CGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285139_24285140insGGG , CM000669.2:g.24285139_24285140insGGG	GRCh38
NC_000007.13:g.24324758_24324759insGGG , CM000669.1:g.24324758_24324759insGGG	GRCh37
NC_000007.12:g.24291283_24291284insGGG	NCBI36
NG_016148.1:g.5952_5953insGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-102_1-101insGGG MANE Select	ENSP00000242152.2:n.1-102_1-101insGGG
ENST00000242152.6:c.1-102_1-101insGGG	ENSP00000242152.2:n.1-102_1-101insGGG
ENST00000405982.1:c.-102_-101insGGG	ENSP00000385282.1:n.-102_-101insGGG
ENST00000407573.5:c.-1+63_-1+64insGGG	ENSP00000384364.1:n.-1+63_-1+64insGGG
NM_000905.3:c.1-102_1-101insGGG	NP_000896.1:n.1-102_1-101insGGG
XM_017012910.1:c.42-29440_42-29439insCCC	XP_016868399.1:n.42-29440_42-29439insCCC
XM_017012911.1:c.42-29440_42-29439insCCC	XP_016868400.1:n.42-29440_42-29439insCCC
XR_001745121.1:n.473+34218_473+34219insCCC
XR_001745122.1:n.345-88110_345-88109insCCC
XR_001745123.1:n.473+34218_473+34219insCCC
XR_001745124.1:n.473+34218_473+34219insCCC
XR_001745125.1:n.473+34218_473+34219insCCC
XR_001745126.1:n.473+34218_473+34219insCCC
XR_001745127.1:n.345-29440_345-29439insCCC
XR_001745129.1:n.473+34218_473+34219insCCC
XR_001745130.1:n.473+34218_473+34219insCCC
XR_001745131.1:n.473+34218_473+34219insCCC
XR_001745132.1:n.473+34218_473+34219insCCC
NM_000905.4:c.1-102_1-101insGGG MANE Select	NP_000896.1:n.1-102_1-101insGGG