Canonical Allele Identifier: CA1694876959

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290776_24290777delinsAT , CM000669.2:g.24290776_24290777delinsAT	GRCh38
NC_000007.13:g.24330395_24330396delinsAT , CM000669.1:g.24330395_24330396delinsAT	GRCh37
NC_000007.12:g.24296920_24296921delinsAT	NCBI36
NG_016148.1:g.11589_11590delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-887_270-886delinsAT MANE Select	ENSP00000242152.2:n.270-887_270-886delinsAT
ENST00000242152.6:c.270-887_270-886delinsAT	ENSP00000242152.2:n.270-887_270-886delinsAT
ENST00000405982.1:c.270-887_270-886delinsAT	ENSP00000385282.1:n.270-887_270-886delinsAT
ENST00000407573.5:c.270-887_270-886delinsAT	ENSP00000384364.1:n.270-887_270-886delinsAT
NM_000905.3:c.270-887_270-886delinsAT	NP_000896.1:n.270-887_270-886delinsAT
XM_017012910.1:c.41+28580_41+28581delinsAT	XP_016868399.1:n.41+28580_41+28581delinsAT
XM_017012911.1:c.41+28580_41+28581delinsAT	XP_016868400.1:n.41+28580_41+28581delinsAT
XR_001745121.1:n.473+28580_473+28581delinsAT
XR_001745122.1:n.345-93748_345-93747delinsAT
XR_001745123.1:n.473+28580_473+28581delinsAT
XR_001745124.1:n.473+28580_473+28581delinsAT
XR_001745125.1:n.473+28580_473+28581delinsAT
XR_001745126.1:n.473+28580_473+28581delinsAT
XR_001745127.1:n.345-35078_345-35077delinsAT
XR_001745129.1:n.473+28580_473+28581delinsAT
XR_001745130.1:n.473+28580_473+28581delinsAT
XR_001745131.1:n.473+28580_473+28581delinsAT
XR_001745132.1:n.473+28580_473+28581delinsAT
NM_000905.4:c.270-887_270-886delinsAT MANE Select	NP_000896.1:n.270-887_270-886delinsAT