Canonical Allele Identifier: CA367052268

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24331295G>A (hg19) ; chr7:g.24291676G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291676G>A , CM000669.2:g.24291676G>A	GRCh38
NC_000007.13:g.24331295G>A , CM000669.1:g.24331295G>A	GRCh37
NC_000007.12:g.24297820G>A	NCBI36
NG_016148.1:g.12489G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.283G>A MANE Select	ENSP00000242152.2:p.Ala95Thr
ENST00000242152.6:c.283G>A	ENSP00000242152.2:p.Ala95Thr
ENST00000405982.1:c.283G>A	ENSP00000385282.1:p.Ala95Thr
ENST00000407573.5:c.283G>A	ENSP00000384364.1:p.Ala95Thr
NM_000905.3:c.283G>A	NP_000896.1:p.Ala95Thr
XM_017012910.1:c.41+27681C>T	XP_016868399.1:n.41+27681C>T
XM_017012911.1:c.41+27681C>T	XP_016868400.1:n.41+27681C>T
XR_001745121.1:n.473+27681C>T
XR_001745122.1:n.345-94647C>T
XR_001745123.1:n.473+27681C>T
XR_001745124.1:n.473+27681C>T
XR_001745125.1:n.473+27681C>T
XR_001745126.1:n.473+27681C>T
XR_001745127.1:n.345-35977C>T
XR_001745129.1:n.473+27681C>T
XR_001745130.1:n.473+27681C>T
XR_001745131.1:n.473+27681C>T
XR_001745132.1:n.473+27681C>T
NM_000905.4:c.283G>A MANE Select	NP_000896.1:p.Ala95Thr