Canonical Allele Identifier: CA1694874346
Gene: NPY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24285300G= , CM000669.2:g.24285300G= GRCh38
NC_000007.13:g.24324919G= , CM000669.1:g.24324919G= GRCh37
NC_000007.12:g.24291444G= NCBI36
NG_016148.1:g.6113G=

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.60G= MANE Select ENSP00000242152.2:p.Val20=
ENST00000242152.6:c.60G= ENSP00000242152.2:p.Val20=
ENST00000405982.1:c.60G= ENSP00000385282.1:p.Val20=
ENST00000407573.5:c.60G= ENSP00000384364.1:p.Val20=
NM_000905.3:c.60G= NP_000896.1:p.Val20=
XM_017012910.1:c.42-29601C= XP_016868399.1:n.42-29601C=
XM_017012911.1:c.42-29601C= XP_016868400.1:n.42-29601C=
XR_001745121.1:n.473+34057C=
XR_001745122.1:n.345-88271C=
XR_001745123.1:n.473+34057C=
XR_001745124.1:n.473+34057C=
XR_001745125.1:n.473+34057C=
XR_001745126.1:n.473+34057C=
XR_001745127.1:n.345-29601C=
XR_001745129.1:n.473+34057C=
XR_001745130.1:n.473+34057C=
XR_001745131.1:n.473+34057C=
XR_001745132.1:n.473+34057C=
NM_000905.4:c.60G= MANE Select NP_000896.1:p.Val20=