Canonical Allele Identifier: CA1694874339

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285290C= , CM000669.2:g.24285290C=	GRCh38
NC_000007.13:g.24324909C= , CM000669.1:g.24324909C=	GRCh37
NC_000007.12:g.24291434C=	NCBI36
NG_016148.1:g.6103C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.50C= MANE Select	ENSP00000242152.2:p.Ser17=
ENST00000242152.6:c.50C=	ENSP00000242152.2:p.Ser17=
ENST00000405982.1:c.50C=	ENSP00000385282.1:p.Ser17=
ENST00000407573.5:c.50C=	ENSP00000384364.1:p.Ser17=
NM_000905.3:c.50C=	NP_000896.1:p.Ser17=
XM_017012910.1:c.42-29591G=	XP_016868399.1:n.42-29591G=
XM_017012911.1:c.42-29591G=	XP_016868400.1:n.42-29591G=
XR_001745121.1:n.473+34067G=
XR_001745122.1:n.345-88261G=
XR_001745123.1:n.473+34067G=
XR_001745124.1:n.473+34067G=
XR_001745125.1:n.473+34067G=
XR_001745126.1:n.473+34067G=
XR_001745127.1:n.345-29591G=
XR_001745129.1:n.473+34067G=
XR_001745130.1:n.473+34067G=
XR_001745131.1:n.473+34067G=
XR_001745132.1:n.473+34067G=
NM_000905.4:c.50C= MANE Select	NP_000896.1:p.Ser17=