Canonical Allele Identifier: CA573757814

Gene: NPY

Linked Data

• dbSNP Id: rs1486037281
• gnomAD v2: 7-24324781-C-CG
• gnomAD v3: 7-24285162-C-CG
• gnomAD v4: 7-24285162-C-CG
• MyVariant Identifiers: chr7:g.24324781_24324782insG (hg19) ; chr7:g.24285162_24285163insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285168dup , CM000669.2:g.24285168dup	GRCh38
NC_000007.13:g.24324787dup , CM000669.1:g.24324787dup	GRCh37
NC_000007.12:g.24291312dup	NCBI36
NG_016148.1:g.5981dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-73dup MANE Select	ENSP00000242152.2:n.1-73dup
ENST00000242152.6:c.1-73dup	ENSP00000242152.2:n.1-73dup
ENST00000405982.1:c.-73dup	ENSP00000385282.1:n.-73dup
ENST00000407573.5:c.1-73dup	ENSP00000384364.1:n.1-73dup
NM_000905.3:c.1-73dup	NP_000896.1:n.1-73dup
XM_017012910.1:c.42-29464dup	XP_016868399.1:n.42-29464dup
XM_017012911.1:c.42-29464dup	XP_016868400.1:n.42-29464dup
XR_001745121.1:n.473+34194dup
XR_001745122.1:n.345-88134dup
XR_001745123.1:n.473+34194dup
XR_001745124.1:n.473+34194dup
XR_001745125.1:n.473+34194dup
XR_001745126.1:n.473+34194dup
XR_001745127.1:n.345-29464dup
XR_001745129.1:n.473+34194dup
XR_001745130.1:n.473+34194dup
XR_001745131.1:n.473+34194dup
XR_001745132.1:n.473+34194dup
NM_000905.4:c.1-73dup MANE Select	NP_000896.1:n.1-73dup