Canonical Allele Identifier: CA4190725

Gene: NPY

Linked Data

• ClinVar Variation Id: 2557274
• ClinVar RCV Id: RCV004323321
• dbSNP Id: rs772669223
• ExAC: 7:24324893 C / A
• gnomAD v2: 7-24324893-C-A
• gnomAD v4: 7-24285274-C-A
• MyVariant Identifiers: chr7:g.24324893C>A (hg19) ; chr7:g.24285274C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285274C>A , CM000669.2:g.24285274C>A	GRCh38
NC_000007.13:g.24324893C>A , CM000669.1:g.24324893C>A	GRCh37
NC_000007.12:g.24291418C>A	NCBI36
NG_016148.1:g.6087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.34C>A MANE Select	ENSP00000242152.2:p.Leu12Met
ENST00000242152.6:c.34C>A	ENSP00000242152.2:p.Leu12Met
ENST00000405982.1:c.34C>A	ENSP00000385282.1:p.Leu12Met
ENST00000407573.5:c.34C>A	ENSP00000384364.1:p.Leu12Met
NM_000905.3:c.34C>A	NP_000896.1:p.Leu12Met
XM_017012910.1:c.42-29575G>T	XP_016868399.1:n.42-29575G>T
XM_017012911.1:c.42-29575G>T	XP_016868400.1:n.42-29575G>T
XR_001745121.1:n.473+34083G>T
XR_001745122.1:n.345-88245G>T
XR_001745123.1:n.473+34083G>T
XR_001745124.1:n.473+34083G>T
XR_001745125.1:n.473+34083G>T
XR_001745126.1:n.473+34083G>T
XR_001745127.1:n.345-29575G>T
XR_001745129.1:n.473+34083G>T
XR_001745130.1:n.473+34083G>T
XR_001745131.1:n.473+34083G>T
XR_001745132.1:n.473+34083G>T
NM_000905.4:c.34C>A MANE Select	NP_000896.1:p.Leu12Met