Canonical Allele Identifier: CA1694876845

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290564_24290565delinsGT , CM000669.2:g.24290564_24290565delinsGT	GRCh38
NC_000007.13:g.24330183_24330184delinsGT , CM000669.1:g.24330183_24330184delinsGT	GRCh37
NC_000007.12:g.24296708_24296709delinsGT	NCBI36
NG_016148.1:g.11377_11378delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+985_269+986delinsGT MANE Select	ENSP00000242152.2:n.269+985_269+986delinsGT
ENST00000242152.6:c.269+985_269+986delinsGT	ENSP00000242152.2:n.269+985_269+986delinsGT
ENST00000405982.1:c.269+985_269+986delinsGT	ENSP00000385282.1:n.269+985_269+986delinsGT
ENST00000407573.5:c.269+985_269+986delinsGT	ENSP00000384364.1:n.269+985_269+986delinsGT
NM_000905.3:c.269+985_269+986delinsGT	NP_000896.1:n.269+985_269+986delinsGT
XM_017012910.1:c.41+28792_41+28793delinsAC	XP_016868399.1:n.41+28792_41+28793delinsAC
XM_017012911.1:c.41+28792_41+28793delinsAC	XP_016868400.1:n.41+28792_41+28793delinsAC
XR_001745121.1:n.473+28792_473+28793delinsAC
XR_001745122.1:n.345-93536_345-93535delinsAC
XR_001745123.1:n.473+28792_473+28793delinsAC
XR_001745124.1:n.473+28792_473+28793delinsAC
XR_001745125.1:n.473+28792_473+28793delinsAC
XR_001745126.1:n.473+28792_473+28793delinsAC
XR_001745127.1:n.345-34866_345-34865delinsAC
XR_001745129.1:n.473+28792_473+28793delinsAC
XR_001745130.1:n.473+28792_473+28793delinsAC
XR_001745131.1:n.473+28792_473+28793delinsAC
XR_001745132.1:n.473+28792_473+28793delinsAC
NM_000905.4:c.269+985_269+986delinsGT MANE Select	NP_000896.1:n.269+985_269+986delinsGT