Canonical Allele Identifier: CA2682048914

Gene: NPY

Linked Data

• gnomAD v4: 7-24291831-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291831_24291832insC , CM000669.2:g.24291831_24291832insC	GRCh38
NC_000007.13:g.24331450_24331451insC , CM000669.1:g.24331450_24331451insC	GRCh37
NC_000007.12:g.24297975_24297976insC	NCBI36
NG_016148.1:g.12644_12645insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*144_*145insC MANE Select	ENSP00000242152.2:n.*144_*145insC
ENST00000242152.6:c.*144_*145insC	ENSP00000242152.2:n.*144_*145insC
NM_000905.3:c.*144_*145insC	NP_000896.1:n.*144_*145insC
XM_017012910.1:c.41+27525_41+27526insG	XP_016868399.1:n.41+27525_41+27526insG
XM_017012911.1:c.41+27525_41+27526insG	XP_016868400.1:n.41+27525_41+27526insG
XR_001745121.1:n.473+27525_473+27526insG
XR_001745122.1:n.345-94803_345-94802insG
XR_001745123.1:n.473+27525_473+27526insG
XR_001745124.1:n.473+27525_473+27526insG
XR_001745125.1:n.473+27525_473+27526insG
XR_001745126.1:n.473+27525_473+27526insG
XR_001745127.1:n.345-36133_345-36132insG
XR_001745129.1:n.473+27525_473+27526insG
XR_001745130.1:n.473+27525_473+27526insG
XR_001745131.1:n.473+27525_473+27526insG
XR_001745132.1:n.473+27525_473+27526insG
NM_000905.4:c.*144_*145insC MANE Select	NP_000896.1:n.*144_*145insC