Canonical Allele Identifier: CA1694877421

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291696G= , CM000669.2:g.24291696G=	GRCh38
NC_000007.13:g.24331315G= , CM000669.1:g.24331315G=	GRCh37
NC_000007.12:g.24297840G=	NCBI36
NG_016148.1:g.12509G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*9G= MANE Select	ENSP00000242152.2:n.*9G=
ENST00000242152.6:c.*9G=	ENSP00000242152.2:n.*9G=
ENST00000405982.1:c.*9G=	ENSP00000385282.1:n.*9G=
ENST00000407573.5:c.*9G=	ENSP00000384364.1:n.*9G=
NM_000905.3:c.*9G=	NP_000896.1:n.*9G=
XM_017012910.1:c.41+27661C=	XP_016868399.1:n.41+27661C=
XM_017012911.1:c.41+27661C=	XP_016868400.1:n.41+27661C=
XR_001745121.1:n.473+27661C=
XR_001745122.1:n.345-94667C=
XR_001745123.1:n.473+27661C=
XR_001745124.1:n.473+27661C=
XR_001745125.1:n.473+27661C=
XR_001745126.1:n.473+27661C=
XR_001745127.1:n.345-35997C=
XR_001745129.1:n.473+27661C=
XR_001745130.1:n.473+27661C=
XR_001745131.1:n.473+27661C=
XR_001745132.1:n.473+27661C=
NM_000905.4:c.*9G= MANE Select	NP_000896.1:n.*9G=