Canonical Allele Identifier: CA367052261

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24331292C>A (hg19) ; chr7:g.24291673C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291673C>A , CM000669.2:g.24291673C>A	GRCh38
NC_000007.13:g.24331292C>A , CM000669.1:g.24331292C>A	GRCh37
NC_000007.12:g.24297817C>A	NCBI36
NG_016148.1:g.12486C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.280C>A MANE Select	ENSP00000242152.2:p.Pro94Thr
ENST00000242152.6:c.280C>A	ENSP00000242152.2:p.Pro94Thr
ENST00000405982.1:c.280C>A	ENSP00000385282.1:p.Pro94Thr
ENST00000407573.5:c.280C>A	ENSP00000384364.1:p.Pro94Thr
NM_000905.3:c.280C>A	NP_000896.1:p.Pro94Thr
XM_017012910.1:c.41+27684G>T	XP_016868399.1:n.41+27684G>T
XM_017012911.1:c.41+27684G>T	XP_016868400.1:n.41+27684G>T
XR_001745121.1:n.473+27684G>T
XR_001745122.1:n.345-94644G>T
XR_001745123.1:n.473+27684G>T
XR_001745124.1:n.473+27684G>T
XR_001745125.1:n.473+27684G>T
XR_001745126.1:n.473+27684G>T
XR_001745127.1:n.345-35974G>T
XR_001745129.1:n.473+27684G>T
XR_001745130.1:n.473+27684G>T
XR_001745131.1:n.473+27684G>T
XR_001745132.1:n.473+27684G>T
NM_000905.4:c.280C>A MANE Select	NP_000896.1:p.Pro94Thr