Canonical Allele Identifier: CA836897965

Gene: NPY

Linked Data

• dbSNP Id: rs1554351544
• MyVariant Identifiers: chr7:g.24330388_24330389insATTATTATT (hg19) ; chr7:g.24290769_24290770insATTATTATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290771_24290772insTATTATTAT , CM000669.2:g.24290771_24290772insTATTATTAT	GRCh38
NC_000007.13:g.24330390_24330391insTATTATTAT , CM000669.1:g.24330390_24330391insTATTATTAT	GRCh37
NC_000007.12:g.24296915_24296916insTATTATTAT	NCBI36
NG_016148.1:g.11584_11585insTATTATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-892_270-891insTATTATTAT MANE Select	ENSP00000242152.2:n.270-892_270-891insTATTATTAT
ENST00000242152.6:c.270-892_270-891insTATTATTAT	ENSP00000242152.2:n.270-892_270-891insTATTATTAT
ENST00000405982.1:c.270-892_270-891insTATTATTAT	ENSP00000385282.1:n.270-892_270-891insTATTATTAT
ENST00000407573.5:c.270-892_270-891insTATTATTAT	ENSP00000384364.1:n.270-892_270-891insTATTATTAT
NM_000905.3:c.270-892_270-891insTATTATTAT	NP_000896.1:n.270-892_270-891insTATTATTAT
XM_017012910.1:c.41+28587_41+28588insAATAATAAT	XP_016868399.1:n.41+28587_41+28588insAATAATAAT
XM_017012911.1:c.41+28587_41+28588insAATAATAAT	XP_016868400.1:n.41+28587_41+28588insAATAATAAT
XR_001745121.1:n.473+28587_473+28588insAATAATAAT
XR_001745122.1:n.345-93741_345-93740insAATAATAAT
XR_001745123.1:n.473+28587_473+28588insAATAATAAT
XR_001745124.1:n.473+28587_473+28588insAATAATAAT
XR_001745125.1:n.473+28587_473+28588insAATAATAAT
XR_001745126.1:n.473+28587_473+28588insAATAATAAT
XR_001745127.1:n.345-35071_345-35070insAATAATAAT
XR_001745129.1:n.473+28587_473+28588insAATAATAAT
XR_001745130.1:n.473+28587_473+28588insAATAATAAT
XR_001745131.1:n.473+28587_473+28588insAATAATAAT
XR_001745132.1:n.473+28587_473+28588insAATAATAAT
NM_000905.4:c.270-892_270-891insTATTATTAT MANE Select	NP_000896.1:n.270-892_270-891insTATTATTAT