Canonical Allele Identifier: CA2682048920

Gene: NPY

Linked Data

• gnomAD v4: 7-24291838-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291841dup , CM000669.2:g.24291841dup	GRCh38
NC_000007.13:g.24331460dup , CM000669.1:g.24331460dup	GRCh37
NC_000007.12:g.24297985dup	NCBI36
NG_016148.1:g.12654dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*154dup MANE Select	ENSP00000242152.2:n.*154dup
ENST00000242152.6:c.*154dup	ENSP00000242152.2:n.*154dup
NM_000905.3:c.*154dup	NP_000896.1:n.*154dup
XM_017012910.1:c.41+27518dup	XP_016868399.1:n.41+27518dup
XM_017012911.1:c.41+27518dup	XP_016868400.1:n.41+27518dup
XR_001745121.1:n.473+27518dup
XR_001745122.1:n.345-94810dup
XR_001745123.1:n.473+27518dup
XR_001745124.1:n.473+27518dup
XR_001745125.1:n.473+27518dup
XR_001745126.1:n.473+27518dup
XR_001745127.1:n.345-36140dup
XR_001745129.1:n.473+27518dup
XR_001745130.1:n.473+27518dup
XR_001745131.1:n.473+27518dup
XR_001745132.1:n.473+27518dup
NM_000905.4:c.*154dup MANE Select	NP_000896.1:n.*154dup