Canonical Allele Identifier: CA155829709

Gene: NPY

Linked Data

• dbSNP Id: rs112454690
• MyVariant Identifiers: chr7:g.24330394_24330395insAAT (hg19) ; chr7:g.24290775_24290776insAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290776_24290777insATA , CM000669.2:g.24290776_24290777insATA	GRCh38
NC_000007.13:g.24330395_24330396insATA , CM000669.1:g.24330395_24330396insATA	GRCh37
NC_000007.12:g.24296920_24296921insATA	NCBI36
NG_016148.1:g.11589_11590insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-887_270-886insATA MANE Select	ENSP00000242152.2:n.270-887_270-886insATA
ENST00000242152.6:c.270-887_270-886insATA	ENSP00000242152.2:n.270-887_270-886insATA
ENST00000405982.1:c.270-887_270-886insATA	ENSP00000385282.1:n.270-887_270-886insATA
ENST00000407573.5:c.270-887_270-886insATA	ENSP00000384364.1:n.270-887_270-886insATA
NM_000905.3:c.270-887_270-886insATA	NP_000896.1:n.270-887_270-886insATA
XM_017012910.1:c.41+28581_41+28582insATT	XP_016868399.1:n.41+28581_41+28582insATT
XM_017012911.1:c.41+28581_41+28582insATT	XP_016868400.1:n.41+28581_41+28582insATT
XR_001745121.1:n.473+28581_473+28582insATT
XR_001745122.1:n.345-93747_345-93746insATT
XR_001745123.1:n.473+28581_473+28582insATT
XR_001745124.1:n.473+28581_473+28582insATT
XR_001745125.1:n.473+28581_473+28582insATT
XR_001745126.1:n.473+28581_473+28582insATT
XR_001745127.1:n.345-35077_345-35076insATT
XR_001745129.1:n.473+28581_473+28582insATT
XR_001745130.1:n.473+28581_473+28582insATT
XR_001745131.1:n.473+28581_473+28582insATT
XR_001745132.1:n.473+28581_473+28582insATT
NM_000905.4:c.270-887_270-886insATA MANE Select	NP_000896.1:n.270-887_270-886insATA