Canonical Allele Identifier: CA2682047954

Gene: NPY

Linked Data

• gnomAD v4: 7-24285010-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285012dup , CM000669.2:g.24285012dup	GRCh38
NC_000007.13:g.24324631dup , CM000669.1:g.24324631dup	GRCh37
NC_000007.12:g.24291156dup	NCBI36
NG_016148.1:g.5825dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-229dup MANE Select	ENSP00000242152.2:n.1-229dup
ENST00000242152.6:c.1-229dup	ENSP00000242152.2:n.1-229dup
ENST00000407573.5:c.-65dup	ENSP00000384364.1:n.-65dup
NM_000905.3:c.1-229dup	NP_000896.1:n.1-229dup
XM_017012910.1:c.42-29312dup	XP_016868399.1:n.42-29312dup
XM_017012911.1:c.42-29312dup	XP_016868400.1:n.42-29312dup
XR_001745121.1:n.473+34346dup
XR_001745122.1:n.345-87982dup
XR_001745123.1:n.473+34346dup
XR_001745124.1:n.473+34346dup
XR_001745125.1:n.473+34346dup
XR_001745126.1:n.473+34346dup
XR_001745127.1:n.345-29312dup
XR_001745129.1:n.473+34346dup
XR_001745130.1:n.473+34346dup
XR_001745131.1:n.473+34346dup
XR_001745132.1:n.473+34346dup
NM_000905.4:c.1-229dup MANE Select	NP_000896.1:n.1-229dup