Canonical Allele Identifier: CA2682048679
Gene: NPY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291516_24291526del , CM000669.2:g.24291516_24291526del GRCh38
NC_000007.13:g.24331135_24331145del , CM000669.1:g.24331135_24331145del GRCh37
NC_000007.12:g.24297660_24297670del NCBI36
NG_016148.1:g.12329_12339del

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.270-147_270-137del MANE Select ENSP00000242152.2:n.270-147_270-137del
ENST00000242152.6:c.270-147_270-137del ENSP00000242152.2:n.270-147_270-137del
ENST00000405982.1:c.270-147_270-137del ENSP00000385282.1:n.270-147_270-137del
ENST00000407573.5:c.270-147_270-137del ENSP00000384364.1:n.270-147_270-137del
NM_000905.3:c.270-147_270-137del NP_000896.1:n.270-147_270-137del
XM_017012910.1:c.41+27834_41+27844del XP_016868399.1:n.41+27834_41+27844del
XM_017012911.1:c.41+27834_41+27844del XP_016868400.1:n.41+27834_41+27844del
XR_001745121.1:n.473+27834_473+27844del
XR_001745122.1:n.345-94494_345-94484del
XR_001745123.1:n.473+27834_473+27844del
XR_001745124.1:n.473+27834_473+27844del
XR_001745125.1:n.473+27834_473+27844del
XR_001745126.1:n.473+27834_473+27844del
XR_001745127.1:n.345-35824_345-35814del
XR_001745129.1:n.473+27834_473+27844del
XR_001745130.1:n.473+27834_473+27844del
XR_001745131.1:n.473+27834_473+27844del
XR_001745132.1:n.473+27834_473+27844del
NM_000905.4:c.270-147_270-137del MANE Select NP_000896.1:n.270-147_270-137del