Canonical Allele Identifier: CA836897720

Gene: NPY

Linked Data

• dbSNP Id: rs1301299643
• MyVariant Identifiers: chr7:g.24330026_24330047del (hg19) ; chr7:g.24290407_24290428del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290417_24290438del , CM000669.2:g.24290417_24290438del	GRCh38
NC_000007.13:g.24330036_24330057del , CM000669.1:g.24330036_24330057del	GRCh37
NC_000007.12:g.24296561_24296582del	NCBI36
NG_016148.1:g.11230_11251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+838_269+859del MANE Select	ENSP00000242152.2:n.269+838_269+859del
ENST00000242152.6:c.269+838_269+859del	ENSP00000242152.2:n.269+838_269+859del
ENST00000405982.1:c.269+838_269+859del	ENSP00000385282.1:n.269+838_269+859del
ENST00000407573.5:c.269+838_269+859del	ENSP00000384364.1:n.269+838_269+859del
NM_000905.3:c.269+838_269+859del	NP_000896.1:n.269+838_269+859del
XM_017012910.1:c.41+28929_41+28950del	XP_016868399.1:n.41+28929_41+28950del
XM_017012911.1:c.41+28929_41+28950del	XP_016868400.1:n.41+28929_41+28950del
XR_001745121.1:n.473+28929_473+28950del
XR_001745122.1:n.345-93399_345-93378del
XR_001745123.1:n.473+28929_473+28950del
XR_001745124.1:n.473+28929_473+28950del
XR_001745125.1:n.473+28929_473+28950del
XR_001745126.1:n.473+28929_473+28950del
XR_001745127.1:n.345-34729_345-34708del
XR_001745129.1:n.473+28929_473+28950del
XR_001745130.1:n.473+28929_473+28950del
XR_001745131.1:n.473+28929_473+28950del
XR_001745132.1:n.473+28929_473+28950del
NM_000905.4:c.269+838_269+859del MANE Select	NP_000896.1:n.269+838_269+859del