Canonical Allele Identifier: CA836898738

Gene: NPY

Linked Data

• dbSNP Id: rs1446384348
• MyVariant Identifiers: chr7:g.24331263_24331264insA (hg19) ; chr7:g.24291644_24291645insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291644_24291645insA , CM000669.2:g.24291644_24291645insA	GRCh38
NC_000007.13:g.24331263_24331264insA , CM000669.1:g.24331263_24331264insA	GRCh37
NC_000007.12:g.24297788_24297789insA	NCBI36
NG_016148.1:g.12457_12458insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-19_270-18insA MANE Select	ENSP00000242152.2:n.270-19_270-18insA
ENST00000242152.6:c.270-19_270-18insA	ENSP00000242152.2:n.270-19_270-18insA
ENST00000405982.1:c.270-19_270-18insA	ENSP00000385282.1:n.270-19_270-18insA
ENST00000407573.5:c.270-19_270-18insA	ENSP00000384364.1:n.270-19_270-18insA
NM_000905.3:c.270-19_270-18insA	NP_000896.1:n.270-19_270-18insA
XM_017012910.1:c.41+27712_41+27713insT	XP_016868399.1:n.41+27712_41+27713insT
XM_017012911.1:c.41+27712_41+27713insT	XP_016868400.1:n.41+27712_41+27713insT
XR_001745121.1:n.473+27712_473+27713insT
XR_001745122.1:n.345-94616_345-94615insT
XR_001745123.1:n.473+27712_473+27713insT
XR_001745124.1:n.473+27712_473+27713insT
XR_001745125.1:n.473+27712_473+27713insT
XR_001745126.1:n.473+27712_473+27713insT
XR_001745127.1:n.345-35946_345-35945insT
XR_001745129.1:n.473+27712_473+27713insT
XR_001745130.1:n.473+27712_473+27713insT
XR_001745131.1:n.473+27712_473+27713insT
XR_001745132.1:n.473+27712_473+27713insT
NM_000905.4:c.270-19_270-18insA MANE Select	NP_000896.1:n.270-19_270-18insA