Canonical Allele Identifier: CA2682048917

Gene: NPY

Linked Data

• gnomAD v4: 7-24291835-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291838del , CM000669.2:g.24291838del	GRCh38
NC_000007.13:g.24331457del , CM000669.1:g.24331457del	GRCh37
NC_000007.12:g.24297982del	NCBI36
NG_016148.1:g.12651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*151del MANE Select	ENSP00000242152.2:n.*151del
ENST00000242152.6:c.*151del	ENSP00000242152.2:n.*151del
NM_000905.3:c.*151del	NP_000896.1:n.*151del
XM_017012910.1:c.41+27521del	XP_016868399.1:n.41+27521del
XM_017012911.1:c.41+27521del	XP_016868400.1:n.41+27521del
XR_001745121.1:n.473+27521del
XR_001745122.1:n.345-94807del
XR_001745123.1:n.473+27521del
XR_001745124.1:n.473+27521del
XR_001745125.1:n.473+27521del
XR_001745126.1:n.473+27521del
XR_001745127.1:n.345-36137del
XR_001745129.1:n.473+27521del
XR_001745130.1:n.473+27521del
XR_001745131.1:n.473+27521del
XR_001745132.1:n.473+27521del
NM_000905.4:c.*151del MANE Select	NP_000896.1:n.*151del