Canonical Allele Identifier: CA1694877493

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291856T= , CM000669.2:g.24291856T=	GRCh38
NC_000007.13:g.24331475T= , CM000669.1:g.24331475T=	GRCh37
NC_000007.12:g.24298000T=	NCBI36
NG_016148.1:g.12669T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*169T= MANE Select	ENSP00000242152.2:n.*169T=
ENST00000242152.6:c.*169T=	ENSP00000242152.2:n.*169T=
NM_000905.3:c.*169T=	NP_000896.1:n.*169T=
XM_017012910.1:c.41+27501A=	XP_016868399.1:n.41+27501A=
XM_017012911.1:c.41+27501A=	XP_016868400.1:n.41+27501A=
XR_001745121.1:n.473+27501A=
XR_001745122.1:n.345-94827A=
XR_001745123.1:n.473+27501A=
XR_001745124.1:n.473+27501A=
XR_001745125.1:n.473+27501A=
XR_001745126.1:n.473+27501A=
XR_001745127.1:n.345-36157A=
XR_001745129.1:n.473+27501A=
XR_001745130.1:n.473+27501A=
XR_001745131.1:n.473+27501A=
XR_001745132.1:n.473+27501A=
NM_000905.4:c.*169T= MANE Select	NP_000896.1:n.*169T=