Canonical Allele Identifier: CA651348257

Gene: NPY

Linked Data

• COSMIC: COSN20862723

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285213_24285214insA , CM000669.2:g.24285213_24285214insA	GRCh38
NC_000007.13:g.24324832_24324833insA , CM000669.1:g.24324832_24324833insA	GRCh37
NC_000007.12:g.24291357_24291358insA	NCBI36
NG_016148.1:g.6026_6027insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-28_1-27insA MANE Select	ENSP00000242152.2:n.1-28_1-27insA
ENST00000242152.6:c.1-28_1-27insA	ENSP00000242152.2:n.1-28_1-27insA
ENST00000405982.1:c.-28_-27insA	ENSP00000385282.1:n.-28_-27insA
ENST00000407573.5:c.1-28_1-27insA	ENSP00000384364.1:n.1-28_1-27insA
NM_000905.3:c.1-28_1-27insA	NP_000896.1:n.1-28_1-27insA
XM_017012910.1:c.42-29515_42-29514insT	XP_016868399.1:n.42-29515_42-29514insT
XM_017012911.1:c.42-29515_42-29514insT	XP_016868400.1:n.42-29515_42-29514insT
XR_001745121.1:n.473+34143_473+34144insT
XR_001745122.1:n.345-88185_345-88184insT
XR_001745123.1:n.473+34143_473+34144insT
XR_001745124.1:n.473+34143_473+34144insT
XR_001745125.1:n.473+34143_473+34144insT
XR_001745126.1:n.473+34143_473+34144insT
XR_001745127.1:n.345-29515_345-29514insT
XR_001745129.1:n.473+34143_473+34144insT
XR_001745130.1:n.473+34143_473+34144insT
XR_001745131.1:n.473+34143_473+34144insT
XR_001745132.1:n.473+34143_473+34144insT
NM_000905.4:c.1-28_1-27insA MANE Select	NP_000896.1:n.1-28_1-27insA