Canonical Allele Identifier: CA1694874336

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285282C= , CM000669.2:g.24285282C=	GRCh38
NC_000007.13:g.24324901C= , CM000669.1:g.24324901C=	GRCh37
NC_000007.12:g.24291426C=	NCBI36
NG_016148.1:g.6095C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.42C= MANE Select	ENSP00000242152.2:p.Leu14=
ENST00000242152.6:c.42C=	ENSP00000242152.2:p.Leu14=
ENST00000405982.1:c.42C=	ENSP00000385282.1:p.Leu14=
ENST00000407573.5:c.42C=	ENSP00000384364.1:p.Leu14=
NM_000905.3:c.42C=	NP_000896.1:p.Leu14=
XM_017012910.1:c.42-29583G=	XP_016868399.1:n.42-29583G=
XM_017012911.1:c.42-29583G=	XP_016868400.1:n.42-29583G=
XR_001745121.1:n.473+34075G=
XR_001745122.1:n.345-88253G=
XR_001745123.1:n.473+34075G=
XR_001745124.1:n.473+34075G=
XR_001745125.1:n.473+34075G=
XR_001745126.1:n.473+34075G=
XR_001745127.1:n.345-29583G=
XR_001745129.1:n.473+34075G=
XR_001745130.1:n.473+34075G=
XR_001745131.1:n.473+34075G=
XR_001745132.1:n.473+34075G=
NM_000905.4:c.42C= MANE Select	NP_000896.1:p.Leu14=