Canonical Allele Identifier: CA1694876918

Gene: NPY

Linked Data

• dbSNP Id: rs1787568008

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290745_24290748del , CM000669.2:g.24290745_24290748del	GRCh38
NC_000007.13:g.24330364_24330367del , CM000669.1:g.24330364_24330367del	GRCh37
NC_000007.12:g.24296889_24296892del	NCBI36
NG_016148.1:g.11558_11561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-918_270-915del MANE Select	ENSP00000242152.2:n.270-918_270-915del
ENST00000242152.6:c.270-918_270-915del	ENSP00000242152.2:n.270-918_270-915del
ENST00000405982.1:c.270-918_270-915del	ENSP00000385282.1:n.270-918_270-915del
ENST00000407573.5:c.270-918_270-915del	ENSP00000384364.1:n.270-918_270-915del
NM_000905.3:c.270-918_270-915del	NP_000896.1:n.270-918_270-915del
XM_017012910.1:c.41+28610_41+28613del	XP_016868399.1:n.41+28610_41+28613del
XM_017012911.1:c.41+28610_41+28613del	XP_016868400.1:n.41+28610_41+28613del
XR_001745121.1:n.473+28610_473+28613del
XR_001745122.1:n.345-93718_345-93715del
XR_001745123.1:n.473+28610_473+28613del
XR_001745124.1:n.473+28610_473+28613del
XR_001745125.1:n.473+28610_473+28613del
XR_001745126.1:n.473+28610_473+28613del
XR_001745127.1:n.345-35048_345-35045del
XR_001745129.1:n.473+28610_473+28613del
XR_001745130.1:n.473+28610_473+28613del
XR_001745131.1:n.473+28610_473+28613del
XR_001745132.1:n.473+28610_473+28613del
NM_000905.4:c.270-918_270-915del MANE Select	NP_000896.1:n.270-918_270-915del