Canonical Allele Identifier: CA2682047933

Gene: NPY

Linked Data

• gnomAD v4: 7-24284994-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24284997_24284998del , CM000669.2:g.24284997_24284998del	GRCh38
NC_000007.13:g.24324616_24324617del , CM000669.1:g.24324616_24324617del	GRCh37
NC_000007.12:g.24291141_24291142del	NCBI36
NG_016148.1:g.5810_5811del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-244_1-243del MANE Select	ENSP00000242152.2:n.1-244_1-243del
ENST00000242152.6:c.1-244_1-243del	ENSP00000242152.2:n.1-244_1-243del
ENST00000407573.5:c.-80_-79del	ENSP00000384364.1:n.-80_-79del
NM_000905.3:c.1-244_1-243del	NP_000896.1:n.1-244_1-243del
XM_017012910.1:c.42-29297_42-29296del	XP_016868399.1:n.42-29297_42-29296del
XM_017012911.1:c.42-29297_42-29296del	XP_016868400.1:n.42-29297_42-29296del
XR_001745121.1:n.473+34361_473+34362del
XR_001745122.1:n.345-87967_345-87966del
XR_001745123.1:n.473+34361_473+34362del
XR_001745124.1:n.473+34361_473+34362del
XR_001745125.1:n.473+34361_473+34362del
XR_001745126.1:n.473+34361_473+34362del
XR_001745127.1:n.345-29297_345-29296del
XR_001745129.1:n.473+34361_473+34362del
XR_001745130.1:n.473+34361_473+34362del
XR_001745131.1:n.473+34361_473+34362del
XR_001745132.1:n.473+34361_473+34362del
NM_000905.4:c.1-244_1-243del MANE Select	NP_000896.1:n.1-244_1-243del