Canonical Allele Identifier: CA1694874330
Gene: NPY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24285266T= , CM000669.2:g.24285266T= GRCh38
NC_000007.13:g.24324885T= , CM000669.1:g.24324885T= GRCh37
NC_000007.12:g.24291410T= NCBI36
NG_016148.1:g.6079T=

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.26T= MANE Select ENSP00000242152.2:p.Leu9=
ENST00000242152.6:c.26T= ENSP00000242152.2:p.Leu9=
ENST00000405982.1:c.26T= ENSP00000385282.1:p.Leu9=
ENST00000407573.5:c.26T= ENSP00000384364.1:p.Leu9=
NM_000905.3:c.26T= NP_000896.1:p.Leu9=
XM_017012910.1:c.42-29567A= XP_016868399.1:n.42-29567A=
XM_017012911.1:c.42-29567A= XP_016868400.1:n.42-29567A=
XR_001745121.1:n.473+34091A=
XR_001745122.1:n.345-88237A=
XR_001745123.1:n.473+34091A=
XR_001745124.1:n.473+34091A=
XR_001745125.1:n.473+34091A=
XR_001745126.1:n.473+34091A=
XR_001745127.1:n.345-29567A=
XR_001745129.1:n.473+34091A=
XR_001745130.1:n.473+34091A=
XR_001745131.1:n.473+34091A=
XR_001745132.1:n.473+34091A=
NM_000905.4:c.26T= MANE Select NP_000896.1:p.Leu9=