Canonical Allele Identifier: CA1099400847

Gene: NPY

Linked Data

• dbSNP Id: rs1554351567
• gnomAD v3: 7-24290775-A-ATT
• gnomAD v4: 7-24290775-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290775_24290776insTT , CM000669.2:g.24290775_24290776insTT	GRCh38
NC_000007.13:g.24330394_24330395insTT , CM000669.1:g.24330394_24330395insTT	GRCh37
NC_000007.12:g.24296919_24296920insTT	NCBI36
NG_016148.1:g.11588_11589insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-888_270-887insTT MANE Select	ENSP00000242152.2:n.270-888_270-887insTT
ENST00000242152.6:c.270-888_270-887insTT	ENSP00000242152.2:n.270-888_270-887insTT
ENST00000405982.1:c.270-888_270-887insTT	ENSP00000385282.1:n.270-888_270-887insTT
ENST00000407573.5:c.270-888_270-887insTT	ENSP00000384364.1:n.270-888_270-887insTT
NM_000905.3:c.270-888_270-887insTT	NP_000896.1:n.270-888_270-887insTT
XM_017012910.1:c.41+28581_41+28582insAA	XP_016868399.1:n.41+28581_41+28582insAA
XM_017012911.1:c.41+28581_41+28582insAA	XP_016868400.1:n.41+28581_41+28582insAA
XR_001745121.1:n.473+28581_473+28582insAA
XR_001745122.1:n.345-93747_345-93746insAA
XR_001745123.1:n.473+28581_473+28582insAA
XR_001745124.1:n.473+28581_473+28582insAA
XR_001745125.1:n.473+28581_473+28582insAA
XR_001745126.1:n.473+28581_473+28582insAA
XR_001745127.1:n.345-35077_345-35076insAA
XR_001745129.1:n.473+28581_473+28582insAA
XR_001745130.1:n.473+28581_473+28582insAA
XR_001745131.1:n.473+28581_473+28582insAA
XR_001745132.1:n.473+28581_473+28582insAA
NM_000905.4:c.270-888_270-887insTT MANE Select	NP_000896.1:n.270-888_270-887insTT