Canonical Allele Identifier: CA1694876879
Gene: NPY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290636G= , CM000669.2:g.24290636G= GRCh38
NC_000007.13:g.24330255G= , CM000669.1:g.24330255G= GRCh37
NC_000007.12:g.24296780G= NCBI36
NG_016148.1:g.11449G=

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.270-1027G= MANE Select ENSP00000242152.2:n.270-1027G=
ENST00000242152.6:c.270-1027G= ENSP00000242152.2:n.270-1027G=
ENST00000405982.1:c.270-1027G= ENSP00000385282.1:n.270-1027G=
ENST00000407573.5:c.270-1027G= ENSP00000384364.1:n.270-1027G=
NM_000905.3:c.270-1027G= NP_000896.1:n.270-1027G=
XM_017012910.1:c.41+28721C= XP_016868399.1:n.41+28721C=
XM_017012911.1:c.41+28721C= XP_016868400.1:n.41+28721C=
XR_001745121.1:n.473+28721C=
XR_001745122.1:n.345-93607C=
XR_001745123.1:n.473+28721C=
XR_001745124.1:n.473+28721C=
XR_001745125.1:n.473+28721C=
XR_001745126.1:n.473+28721C=
XR_001745127.1:n.345-34937C=
XR_001745129.1:n.473+28721C=
XR_001745130.1:n.473+28721C=
XR_001745131.1:n.473+28721C=
XR_001745132.1:n.473+28721C=
NM_000905.4:c.270-1027G= MANE Select NP_000896.1:n.270-1027G=