Canonical Allele Identifier: CA1694876822
Gene: NPY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290525_24290526delinsAC , CM000669.2:g.24290525_24290526delinsAC GRCh38
NC_000007.13:g.24330144_24330145delinsAC , CM000669.1:g.24330144_24330145delinsAC GRCh37
NC_000007.12:g.24296669_24296670delinsAC NCBI36
NG_016148.1:g.11338_11339delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.269+946_269+947delinsAC MANE Select ENSP00000242152.2:n.269+946_269+947delins...
ENST00000242152.6:c.269+946_269+947delinsAC ENSP00000242152.2:n.269+946_269+947delins...
ENST00000405982.1:c.269+946_269+947delinsAC ENSP00000385282.1:n.269+946_269+947delins...
ENST00000407573.5:c.269+946_269+947delinsAC ENSP00000384364.1:n.269+946_269+947delins...
NM_000905.3:c.269+946_269+947delinsAC NP_000896.1:n.269+946_269+947delinsAC
XM_017012910.1:c.41+28831_41+28832delinsGT XP_016868399.1:n.41+28831_41+28832delinsG...
XM_017012911.1:c.41+28831_41+28832delinsGT XP_016868400.1:n.41+28831_41+28832delinsG...
XR_001745121.1:n.473+28831_473+28832delinsGT
XR_001745122.1:n.345-93497_345-93496delinsGT
XR_001745123.1:n.473+28831_473+28832delinsGT
XR_001745124.1:n.473+28831_473+28832delinsGT
XR_001745125.1:n.473+28831_473+28832delinsGT
XR_001745126.1:n.473+28831_473+28832delinsGT
XR_001745127.1:n.345-34827_345-34826delinsGT
XR_001745129.1:n.473+28831_473+28832delinsGT
XR_001745130.1:n.473+28831_473+28832delinsGT
XR_001745131.1:n.473+28831_473+28832delinsGT
XR_001745132.1:n.473+28831_473+28832delinsGT
NM_000905.4:c.269+946_269+947delinsAC MANE Select NP_000896.1:n.269+946_269+947delinsAC