Canonical Allele Identifier: CA1099400682

Gene: NPY

Linked Data

• dbSNP Id: rs1787558962
• gnomAD v3: 7-24290459-CACTTG-C
• gnomAD v4: 7-24290459-CACTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290460_24290464del , CM000669.2:g.24290460_24290464del	GRCh38
NC_000007.13:g.24330079_24330083del , CM000669.1:g.24330079_24330083del	GRCh37
NC_000007.12:g.24296604_24296608del	NCBI36
NG_016148.1:g.11273_11277del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+881_269+885del MANE Select	ENSP00000242152.2:n.269+881_269+885del
ENST00000242152.6:c.269+881_269+885del	ENSP00000242152.2:n.269+881_269+885del
ENST00000405982.1:c.269+881_269+885del	ENSP00000385282.1:n.269+881_269+885del
ENST00000407573.5:c.269+881_269+885del	ENSP00000384364.1:n.269+881_269+885del
NM_000905.3:c.269+881_269+885del	NP_000896.1:n.269+881_269+885del
XM_017012910.1:c.41+28893_41+28897del	XP_016868399.1:n.41+28893_41+28897del
XM_017012911.1:c.41+28893_41+28897del	XP_016868400.1:n.41+28893_41+28897del
XR_001745121.1:n.473+28893_473+28897del
XR_001745122.1:n.345-93435_345-93431del
XR_001745123.1:n.473+28893_473+28897del
XR_001745124.1:n.473+28893_473+28897del
XR_001745125.1:n.473+28893_473+28897del
XR_001745126.1:n.473+28893_473+28897del
XR_001745127.1:n.345-34765_345-34761del
XR_001745129.1:n.473+28893_473+28897del
XR_001745130.1:n.473+28893_473+28897del
XR_001745131.1:n.473+28893_473+28897del
XR_001745132.1:n.473+28893_473+28897del
NM_000905.4:c.269+881_269+885del MANE Select	NP_000896.1:n.269+881_269+885del