Canonical Allele Identifier: CA2682048915

Gene: NPY

Linked Data

• gnomAD v4: 7-24291833-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291833_24291834insC , CM000669.2:g.24291833_24291834insC	GRCh38
NC_000007.13:g.24331452_24331453insC , CM000669.1:g.24331452_24331453insC	GRCh37
NC_000007.12:g.24297977_24297978insC	NCBI36
NG_016148.1:g.12646_12647insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*146_*147insC MANE Select	ENSP00000242152.2:n.*146_*147insC
ENST00000242152.6:c.*146_*147insC	ENSP00000242152.2:n.*146_*147insC
NM_000905.3:c.*146_*147insC	NP_000896.1:n.*146_*147insC
XM_017012910.1:c.41+27523_41+27524insG	XP_016868399.1:n.41+27523_41+27524insG
XM_017012911.1:c.41+27523_41+27524insG	XP_016868400.1:n.41+27523_41+27524insG
XR_001745121.1:n.473+27523_473+27524insG
XR_001745122.1:n.345-94805_345-94804insG
XR_001745123.1:n.473+27523_473+27524insG
XR_001745124.1:n.473+27523_473+27524insG
XR_001745125.1:n.473+27523_473+27524insG
XR_001745126.1:n.473+27523_473+27524insG
XR_001745127.1:n.345-36135_345-36134insG
XR_001745129.1:n.473+27523_473+27524insG
XR_001745130.1:n.473+27523_473+27524insG
XR_001745131.1:n.473+27523_473+27524insG
XR_001745132.1:n.473+27523_473+27524insG
NM_000905.4:c.*146_*147insC MANE Select	NP_000896.1:n.*146_*147insC