Canonical Allele Identifier: CA2682048912

Gene: NPY

Linked Data

• gnomAD v4: 7-24291829-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291835_24291836del , CM000669.2:g.24291835_24291836del	GRCh38
NC_000007.13:g.24331454_24331455del , CM000669.1:g.24331454_24331455del	GRCh37
NC_000007.12:g.24297979_24297980del	NCBI36
NG_016148.1:g.12648_12649del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*148_*149del MANE Select	ENSP00000242152.2:n.*148_*149del
ENST00000242152.6:c.*148_*149del	ENSP00000242152.2:n.*148_*149del
NM_000905.3:c.*148_*149del	NP_000896.1:n.*148_*149del
XM_017012910.1:c.41+27526_41+27527del	XP_016868399.1:n.41+27526_41+27527del
XM_017012911.1:c.41+27526_41+27527del	XP_016868400.1:n.41+27526_41+27527del
XR_001745121.1:n.473+27526_473+27527del
XR_001745122.1:n.345-94802_345-94801del
XR_001745123.1:n.473+27526_473+27527del
XR_001745124.1:n.473+27526_473+27527del
XR_001745125.1:n.473+27526_473+27527del
XR_001745126.1:n.473+27526_473+27527del
XR_001745127.1:n.345-36132_345-36131del
XR_001745129.1:n.473+27526_473+27527del
XR_001745130.1:n.473+27526_473+27527del
XR_001745131.1:n.473+27526_473+27527del
XR_001745132.1:n.473+27526_473+27527del
NM_000905.4:c.*148_*149del MANE Select	NP_000896.1:n.*148_*149del