Canonical Allele Identifier: CA2682048864

Gene: NPY

Linked Data

• gnomAD v4: 7-24291744-G-GAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291744_24291745insAAAA , CM000669.2:g.24291744_24291745insAAAA	GRCh38
NC_000007.13:g.24331363_24331364insAAAA , CM000669.1:g.24331363_24331364insAAAA	GRCh37
NC_000007.12:g.24297888_24297889insAAAA	NCBI36
NG_016148.1:g.12557_12558insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*57_*58insAAAA MANE Select	ENSP00000242152.2:n.*57_*58insAAAA
ENST00000242152.6:c.*57_*58insAAAA	ENSP00000242152.2:n.*57_*58insAAAA
ENST00000405982.1:c.*57_*58insAAAA	ENSP00000385282.1:n.*57_*58insAAAA
ENST00000407573.5:c.*57_*58insAAAA	ENSP00000384364.1:n.*57_*58insAAAA
NM_000905.3:c.*57_*58insAAAA	NP_000896.1:n.*57_*58insAAAA
XM_017012910.1:c.41+27612_41+27613insTTTT	XP_016868399.1:n.41+27612_41+27613insTTTT
XM_017012911.1:c.41+27612_41+27613insTTTT	XP_016868400.1:n.41+27612_41+27613insTTTT
XR_001745121.1:n.473+27612_473+27613insTTTT
XR_001745122.1:n.345-94716_345-94715insTTTT
XR_001745123.1:n.473+27612_473+27613insTTTT
XR_001745124.1:n.473+27612_473+27613insTTTT
XR_001745125.1:n.473+27612_473+27613insTTTT
XR_001745126.1:n.473+27612_473+27613insTTTT
XR_001745127.1:n.345-36046_345-36045insTTTT
XR_001745129.1:n.473+27612_473+27613insTTTT
XR_001745130.1:n.473+27612_473+27613insTTTT
XR_001745131.1:n.473+27612_473+27613insTTTT
XR_001745132.1:n.473+27612_473+27613insTTTT
NM_000905.4:c.*57_*58insAAAA MANE Select	NP_000896.1:n.*57_*58insAAAA