Canonical Allele Identifier: CA1694874345

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285298G= , CM000669.2:g.24285298G=	GRCh38
NC_000007.13:g.24324917G= , CM000669.1:g.24324917G=	GRCh37
NC_000007.12:g.24291442G=	NCBI36
NG_016148.1:g.6111G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.58G= MANE Select	ENSP00000242152.2:p.Val20=
ENST00000242152.6:c.58G=	ENSP00000242152.2:p.Val20=
ENST00000405982.1:c.58G=	ENSP00000385282.1:p.Val20=
ENST00000407573.5:c.58G=	ENSP00000384364.1:p.Val20=
NM_000905.3:c.58G=	NP_000896.1:p.Val20=
XM_017012910.1:c.42-29599C=	XP_016868399.1:n.42-29599C=
XM_017012911.1:c.42-29599C=	XP_016868400.1:n.42-29599C=
XR_001745121.1:n.473+34059C=
XR_001745122.1:n.345-88269C=
XR_001745123.1:n.473+34059C=
XR_001745124.1:n.473+34059C=
XR_001745125.1:n.473+34059C=
XR_001745126.1:n.473+34059C=
XR_001745127.1:n.345-29599C=
XR_001745129.1:n.473+34059C=
XR_001745130.1:n.473+34059C=
XR_001745131.1:n.473+34059C=
XR_001745132.1:n.473+34059C=
NM_000905.4:c.58G= MANE Select	NP_000896.1:p.Val20=