Canonical Allele Identifier: CA123720
Gene: NPY HGNC NCBI

Linked Data

ClinVar Variation Id: 14024
ClinVar RCV Id: RCV000015068
dbSNP Id: rs16139

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.20T>C MANE Select ENSP00000242152.2:p.Leu7Pro
ENST00000242152.6:c.20T>C ENSP00000242152.2:p.Leu7Pro
ENST00000405982.1:c.20T>C ENSP00000385282.1:p.Leu7Pro
ENST00000407573.5:c.20T>C ENSP00000384364.1:p.Leu7Pro
NM_000905.3:c.20T>C NP_000896.1:p.Leu7Pro
XM_017012910.1:c.42-29561A>G XP_016868399.1:n.42-29561A>G
XM_017012911.1:c.42-29561A>G XP_016868400.1:n.42-29561A>G
XR_001745121.1:n.473+34097A>G
XR_001745122.1:n.345-88231A>G
XR_001745123.1:n.473+34097A>G
XR_001745124.1:n.473+34097A>G
XR_001745125.1:n.473+34097A>G
XR_001745126.1:n.473+34097A>G
XR_001745127.1:n.345-29561A>G
XR_001745129.1:n.473+34097A>G
XR_001745130.1:n.473+34097A>G
XR_001745131.1:n.473+34097A>G
XR_001745132.1:n.473+34097A>G
NM_000905.4:c.20T>C MANE Select NP_000896.1:p.Leu7Pro