Canonical Allele Identifier: CA651348256

Gene: NPY

Linked Data

• COSMIC: COSN18722864

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285205_24285206insA , CM000669.2:g.24285205_24285206insA	GRCh38
NC_000007.13:g.24324824_24324825insA , CM000669.1:g.24324824_24324825insA	GRCh37
NC_000007.12:g.24291349_24291350insA	NCBI36
NG_016148.1:g.6018_6019insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-36_1-35insA MANE Select	ENSP00000242152.2:n.1-36_1-35insA
ENST00000242152.6:c.1-36_1-35insA	ENSP00000242152.2:n.1-36_1-35insA
ENST00000405982.1:c.-36_-35insA	ENSP00000385282.1:n.-36_-35insA
ENST00000407573.5:c.1-36_1-35insA	ENSP00000384364.1:n.1-36_1-35insA
NM_000905.3:c.1-36_1-35insA	NP_000896.1:n.1-36_1-35insA
XM_017012910.1:c.42-29507_42-29506insT	XP_016868399.1:n.42-29507_42-29506insT
XM_017012911.1:c.42-29507_42-29506insT	XP_016868400.1:n.42-29507_42-29506insT
XR_001745121.1:n.473+34151_473+34152insT
XR_001745122.1:n.345-88177_345-88176insT
XR_001745123.1:n.473+34151_473+34152insT
XR_001745124.1:n.473+34151_473+34152insT
XR_001745125.1:n.473+34151_473+34152insT
XR_001745126.1:n.473+34151_473+34152insT
XR_001745127.1:n.345-29507_345-29506insT
XR_001745129.1:n.473+34151_473+34152insT
XR_001745130.1:n.473+34151_473+34152insT
XR_001745131.1:n.473+34151_473+34152insT
XR_001745132.1:n.473+34151_473+34152insT
NM_000905.4:c.1-36_1-35insA MANE Select	NP_000896.1:n.1-36_1-35insA