Canonical Allele Identifier: CA4190722
Gene: NPY HGNC NCBI

Linked Data

dbSNP Id: rs16139

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24285260T>A , CM000669.2:g.24285260T>A GRCh38
NC_000007.13:g.24324879T>A , CM000669.1:g.24324879T>A GRCh37
NC_000007.12:g.24291404T>A NCBI36
NG_016148.1:g.6073T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.20T>A MANE Select ENSP00000242152.2:p.Leu7Gln
ENST00000242152.6:c.20T>A ENSP00000242152.2:p.Leu7Gln
ENST00000405982.1:c.20T>A ENSP00000385282.1:p.Leu7Gln
ENST00000407573.5:c.20T>A ENSP00000384364.1:p.Leu7Gln
NM_000905.3:c.20T>A NP_000896.1:p.Leu7Gln
XM_017012910.1:c.42-29561A>T XP_016868399.1:n.42-29561A>T
XM_017012911.1:c.42-29561A>T XP_016868400.1:n.42-29561A>T
XR_001745121.1:n.473+34097A>T
XR_001745122.1:n.345-88231A>T
XR_001745123.1:n.473+34097A>T
XR_001745124.1:n.473+34097A>T
XR_001745125.1:n.473+34097A>T
XR_001745126.1:n.473+34097A>T
XR_001745127.1:n.345-29561A>T
XR_001745129.1:n.473+34097A>T
XR_001745130.1:n.473+34097A>T
XR_001745131.1:n.473+34097A>T
XR_001745132.1:n.473+34097A>T
NM_000905.4:c.20T>A MANE Select NP_000896.1:p.Leu7Gln