Canonical Allele Identifier: CA1694876791

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290459_24290464delinsCACTTG , CM000669.2:g.24290459_24290464delinsCACTTG	GRCh38
NC_000007.13:g.24330078_24330083delinsCACTTG , CM000669.1:g.24330078_24330083delinsCACTTG	GRCh37
NC_000007.12:g.24296603_24296608delinsCACTTG	NCBI36
NG_016148.1:g.11272_11277delinsCACTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+880_269+885delinsCACTTG MANE Select	ENSP00000242152.2:n.269+880_269+885delinsCACTTG
ENST00000242152.6:c.269+880_269+885delinsCACTTG	ENSP00000242152.2:n.269+880_269+885delinsCACTTG
ENST00000405982.1:c.269+880_269+885delinsCACTTG	ENSP00000385282.1:n.269+880_269+885delinsCACTTG
ENST00000407573.5:c.269+880_269+885delinsCACTTG	ENSP00000384364.1:n.269+880_269+885delinsCACTTG
NM_000905.3:c.269+880_269+885delinsCACTTG	NP_000896.1:n.269+880_269+885delinsCACTTG
XM_017012910.1:c.41+28893_41+28898delinsCAAGTG	XP_016868399.1:n.41+28893_41+28898delinsCAAGTG
XM_017012911.1:c.41+28893_41+28898delinsCAAGTG	XP_016868400.1:n.41+28893_41+28898delinsCAAGTG
XR_001745121.1:n.473+28893_473+28898delinsCAAGTG
XR_001745122.1:n.345-93435_345-93430delinsCAAGTG
XR_001745123.1:n.473+28893_473+28898delinsCAAGTG
XR_001745124.1:n.473+28893_473+28898delinsCAAGTG
XR_001745125.1:n.473+28893_473+28898delinsCAAGTG
XR_001745126.1:n.473+28893_473+28898delinsCAAGTG
XR_001745127.1:n.345-34765_345-34760delinsCAAGTG
XR_001745129.1:n.473+28893_473+28898delinsCAAGTG
XR_001745130.1:n.473+28893_473+28898delinsCAAGTG
XR_001745131.1:n.473+28893_473+28898delinsCAAGTG
XR_001745132.1:n.473+28893_473+28898delinsCAAGTG
NM_000905.4:c.269+880_269+885delinsCACTTG MANE Select	NP_000896.1:n.269+880_269+885delinsCACTTG