Canonical Allele Identifier: CA917964814

Gene: NPY

Linked Data

• dbSNP Id: rs1583576514

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290472_24290475del , CM000669.2:g.24290472_24290475del	GRCh38
NC_000007.13:g.24330091_24330094del , CM000669.1:g.24330091_24330094del	GRCh37
NC_000007.12:g.24296616_24296619del	NCBI36
NG_016148.1:g.11285_11288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+893_269+896del MANE Select	ENSP00000242152.2:n.269+893_269+896del
ENST00000242152.6:c.269+893_269+896del	ENSP00000242152.2:n.269+893_269+896del
ENST00000405982.1:c.269+893_269+896del	ENSP00000385282.1:n.269+893_269+896del
ENST00000407573.5:c.269+893_269+896del	ENSP00000384364.1:n.269+893_269+896del
NM_000905.3:c.269+893_269+896del	NP_000896.1:n.269+893_269+896del
XM_017012910.1:c.41+28886_41+28889del	XP_016868399.1:n.41+28886_41+28889del
XM_017012911.1:c.41+28886_41+28889del	XP_016868400.1:n.41+28886_41+28889del
XR_001745121.1:n.473+28886_473+28889del
XR_001745122.1:n.345-93442_345-93439del
XR_001745123.1:n.473+28886_473+28889del
XR_001745124.1:n.473+28886_473+28889del
XR_001745125.1:n.473+28886_473+28889del
XR_001745126.1:n.473+28886_473+28889del
XR_001745127.1:n.345-34772_345-34769del
XR_001745129.1:n.473+28886_473+28889del
XR_001745130.1:n.473+28886_473+28889del
XR_001745131.1:n.473+28886_473+28889del
XR_001745132.1:n.473+28886_473+28889del
NM_000905.4:c.269+893_269+896del MANE Select	NP_000896.1:n.269+893_269+896del