Canonical Allele Identifier: CA2682048857

Gene: NPY

Linked Data

• gnomAD v4: 7-24291732-ATATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291734_24291737del , CM000669.2:g.24291734_24291737del	GRCh38
NC_000007.13:g.24331353_24331356del , CM000669.1:g.24331353_24331356del	GRCh37
NC_000007.12:g.24297878_24297881del	NCBI36
NG_016148.1:g.12547_12550del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*47_*50del MANE Select	ENSP00000242152.2:n.*47_*50del
ENST00000242152.6:c.*47_*50del	ENSP00000242152.2:n.*47_*50del
ENST00000405982.1:c.*47_*50del	ENSP00000385282.1:n.*47_*50del
ENST00000407573.5:c.*47_*50del	ENSP00000384364.1:n.*47_*50del
NM_000905.3:c.*47_*50del	NP_000896.1:n.*47_*50del
XM_017012910.1:c.41+27621_41+27624del	XP_016868399.1:n.41+27621_41+27624del
XM_017012911.1:c.41+27621_41+27624del	XP_016868400.1:n.41+27621_41+27624del
XR_001745121.1:n.473+27621_473+27624del
XR_001745122.1:n.345-94707_345-94704del
XR_001745123.1:n.473+27621_473+27624del
XR_001745124.1:n.473+27621_473+27624del
XR_001745125.1:n.473+27621_473+27624del
XR_001745126.1:n.473+27621_473+27624del
XR_001745127.1:n.345-36037_345-36034del
XR_001745129.1:n.473+27621_473+27624del
XR_001745130.1:n.473+27621_473+27624del
XR_001745131.1:n.473+27621_473+27624del
XR_001745132.1:n.473+27621_473+27624del
NM_000905.4:c.*47_*50del MANE Select	NP_000896.1:n.*47_*50del