Canonical Allele Identifier: CA1694877478

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291828T= , CM000669.2:g.24291828T=	GRCh38
NC_000007.13:g.24331447T= , CM000669.1:g.24331447T=	GRCh37
NC_000007.12:g.24297972T=	NCBI36
NG_016148.1:g.12641T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*141T= MANE Select	ENSP00000242152.2:n.*141T=
ENST00000242152.6:c.*141T=	ENSP00000242152.2:n.*141T=
NM_000905.3:c.*141T=	NP_000896.1:n.*141T=
XM_017012910.1:c.41+27529A=	XP_016868399.1:n.41+27529A=
XM_017012911.1:c.41+27529A=	XP_016868400.1:n.41+27529A=
XR_001745121.1:n.473+27529A=
XR_001745122.1:n.345-94799A=
XR_001745123.1:n.473+27529A=
XR_001745124.1:n.473+27529A=
XR_001745125.1:n.473+27529A=
XR_001745126.1:n.473+27529A=
XR_001745127.1:n.345-36129A=
XR_001745129.1:n.473+27529A=
XR_001745130.1:n.473+27529A=
XR_001745131.1:n.473+27529A=
XR_001745132.1:n.473+27529A=
NM_000905.4:c.*141T= MANE Select	NP_000896.1:n.*141T=