Canonical Allele Identifier: CA2682048064

Gene: NPY

Linked Data

• gnomAD v4: 7-24285078-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285079_24285080del , CM000669.2:g.24285079_24285080del	GRCh38
NC_000007.13:g.24324698_24324699del , CM000669.1:g.24324698_24324699del	GRCh37
NC_000007.12:g.24291223_24291224del	NCBI36
NG_016148.1:g.5892_5893del

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-162_1-161del MANE Select	ENSP00000242152.2:n.1-162_1-161del
ENST00000242152.6:c.1-162_1-161del	ENSP00000242152.2:n.1-162_1-161del
ENST00000407573.5:c.-1+3_-1+4del	ENSP00000384364.1:n.-1+3_-1+4del
NM_000905.3:c.1-162_1-161del	NP_000896.1:n.1-162_1-161del
XM_017012910.1:c.42-29381_42-29380del	XP_016868399.1:n.42-29381_42-29380del
XM_017012911.1:c.42-29381_42-29380del	XP_016868400.1:n.42-29381_42-29380del
XR_001745121.1:n.473+34277_473+34278del
XR_001745122.1:n.345-88051_345-88050del
XR_001745123.1:n.473+34277_473+34278del
XR_001745124.1:n.473+34277_473+34278del
XR_001745125.1:n.473+34277_473+34278del
XR_001745126.1:n.473+34277_473+34278del
XR_001745127.1:n.345-29381_345-29380del
XR_001745129.1:n.473+34277_473+34278del
XR_001745130.1:n.473+34277_473+34278del
XR_001745131.1:n.473+34277_473+34278del
XR_001745132.1:n.473+34277_473+34278del
NM_000905.4:c.1-162_1-161del MANE Select	NP_000896.1:n.1-162_1-161del