Canonical Allele Identifier: CA836922752

Gene: NPY

Linked Data

• dbSNP Id: rs1229387586
• gnomAD v3: 7-24285129-T-TG
• gnomAD v4: 7-24285129-T-TG
• MyVariant Identifiers: chr7:g.24324748_24324749insG (hg19) ; chr7:g.24285129_24285130insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285134dup , CM000669.2:g.24285134dup	GRCh38
NC_000007.13:g.24324753dup , CM000669.1:g.24324753dup	GRCh37
NC_000007.12:g.24291278dup	NCBI36
NG_016148.1:g.5947dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-107dup MANE Select	ENSP00000242152.2:n.1-107dup
ENST00000242152.6:c.1-107dup	ENSP00000242152.2:n.1-107dup
ENST00000405982.1:c.-107dup	ENSP00000385282.1:n.-107dup
ENST00000407573.5:c.-1+58dup	ENSP00000384364.1:n.-1+58dup
NM_000905.3:c.1-107dup	NP_000896.1:n.1-107dup
XM_017012910.1:c.42-29431dup	XP_016868399.1:n.42-29431dup
XM_017012911.1:c.42-29431dup	XP_016868400.1:n.42-29431dup
XR_001745121.1:n.473+34227dup
XR_001745122.1:n.345-88101dup
XR_001745123.1:n.473+34227dup
XR_001745124.1:n.473+34227dup
XR_001745125.1:n.473+34227dup
XR_001745126.1:n.473+34227dup
XR_001745127.1:n.345-29431dup
XR_001745129.1:n.473+34227dup
XR_001745130.1:n.473+34227dup
XR_001745131.1:n.473+34227dup
XR_001745132.1:n.473+34227dup
NM_000905.4:c.1-107dup MANE Select	NP_000896.1:n.1-107dup