Canonical Allele Identifier: CA1694876794

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290467_24290471delinsCAGTG , CM000669.2:g.24290467_24290471delinsCAGTG	GRCh38
NC_000007.13:g.24330086_24330090delinsCAGTG , CM000669.1:g.24330086_24330090delinsCAGTG	GRCh37
NC_000007.12:g.24296611_24296615delinsCAGTG	NCBI36
NG_016148.1:g.11280_11284delinsCAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+888_269+892delinsCAGTG MANE Select	ENSP00000242152.2:n.269+888_269+892delinsCAGTG
ENST00000242152.6:c.269+888_269+892delinsCAGTG	ENSP00000242152.2:n.269+888_269+892delinsCAGTG
ENST00000405982.1:c.269+888_269+892delinsCAGTG	ENSP00000385282.1:n.269+888_269+892delinsCAGTG
ENST00000407573.5:c.269+888_269+892delinsCAGTG	ENSP00000384364.1:n.269+888_269+892delinsCAGTG
NM_000905.3:c.269+888_269+892delinsCAGTG	NP_000896.1:n.269+888_269+892delinsCAGTG
XM_017012910.1:c.41+28886_41+28890delinsCACTG	XP_016868399.1:n.41+28886_41+28890delinsCACTG
XM_017012911.1:c.41+28886_41+28890delinsCACTG	XP_016868400.1:n.41+28886_41+28890delinsCACTG
XR_001745121.1:n.473+28886_473+28890delinsCACTG
XR_001745122.1:n.345-93442_345-93438delinsCACTG
XR_001745123.1:n.473+28886_473+28890delinsCACTG
XR_001745124.1:n.473+28886_473+28890delinsCACTG
XR_001745125.1:n.473+28886_473+28890delinsCACTG
XR_001745126.1:n.473+28886_473+28890delinsCACTG
XR_001745127.1:n.345-34772_345-34768delinsCACTG
XR_001745129.1:n.473+28886_473+28890delinsCACTG
XR_001745130.1:n.473+28886_473+28890delinsCACTG
XR_001745131.1:n.473+28886_473+28890delinsCACTG
XR_001745132.1:n.473+28886_473+28890delinsCACTG
NM_000905.4:c.269+888_269+892delinsCAGTG MANE Select	NP_000896.1:n.269+888_269+892delinsCAGTG