Canonical Allele Identifier: CA1694877460

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291784A= , CM000669.2:g.24291784A=	GRCh38
NC_000007.13:g.24331403A= , CM000669.1:g.24331403A=	GRCh37
NC_000007.12:g.24297928A=	NCBI36
NG_016148.1:g.12597A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*97A= MANE Select	ENSP00000242152.2:n.*97A=
ENST00000242152.6:c.*97A=	ENSP00000242152.2:n.*97A=
ENST00000405982.1:c.*97A=	ENSP00000385282.1:n.*97A=
ENST00000407573.5:c.*97A=	ENSP00000384364.1:n.*97A=
NM_000905.3:c.*97A=	NP_000896.1:n.*97A=
XM_017012910.1:c.41+27573T=	XP_016868399.1:n.41+27573T=
XM_017012911.1:c.41+27573T=	XP_016868400.1:n.41+27573T=
XR_001745121.1:n.473+27573T=
XR_001745122.1:n.345-94755T=
XR_001745123.1:n.473+27573T=
XR_001745124.1:n.473+27573T=
XR_001745125.1:n.473+27573T=
XR_001745126.1:n.473+27573T=
XR_001745127.1:n.345-36085T=
XR_001745129.1:n.473+27573T=
XR_001745130.1:n.473+27573T=
XR_001745131.1:n.473+27573T=
XR_001745132.1:n.473+27573T=
NM_000905.4:c.*97A= MANE Select	NP_000896.1:n.*97A=