Canonical Allele Identifier: CA2559339696
Gene: NPY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290786_24290787insGATTAT , CM000669.2:g.24290786_24290787insGATTAT GRCh38
NC_000007.13:g.24330405_24330406insGATTAT , CM000669.1:g.24330405_24330406insGATTAT GRCh37
NC_000007.12:g.24296930_24296931insGATTAT NCBI36
NG_016148.1:g.11599_11600insGATTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000242152.7:c.270-877_270-876insGATTAT MANE Select ENSP00000242152.2:n.270-877_270-876insGATTAT
ENST00000242152.6:c.270-877_270-876insGATTAT ENSP00000242152.2:n.270-877_270-876insGATTAT
ENST00000405982.1:c.270-877_270-876insGATTAT ENSP00000385282.1:n.270-877_270-876insGATTAT
ENST00000407573.5:c.270-877_270-876insGATTAT ENSP00000384364.1:n.270-877_270-876insGATTAT
NM_000905.3:c.270-877_270-876insGATTAT NP_000896.1:n.270-877_270-876insGATTAT
XM_017012910.1:c.41+28575_41+28576insCATAAT XP_016868399.1:n.41+28575_41+28576insCATAAT
XM_017012911.1:c.41+28575_41+28576insCATAAT XP_016868400.1:n.41+28575_41+28576insCATAAT
XR_001745121.1:n.473+28575_473+28576insCATAAT
XR_001745122.1:n.345-93753_345-93752insCATAAT
XR_001745123.1:n.473+28575_473+28576insCATAAT
XR_001745124.1:n.473+28575_473+28576insCATAAT
XR_001745125.1:n.473+28575_473+28576insCATAAT
XR_001745126.1:n.473+28575_473+28576insCATAAT
XR_001745127.1:n.345-35083_345-35082insCATAAT
XR_001745129.1:n.473+28575_473+28576insCATAAT
XR_001745130.1:n.473+28575_473+28576insCATAAT
XR_001745131.1:n.473+28575_473+28576insCATAAT
XR_001745132.1:n.473+28575_473+28576insCATAAT
NM_000905.4:c.270-877_270-876insGATTAT MANE Select NP_000896.1:n.270-877_270-876insGATTAT