Canonical Allele Identifier: CA651348254

Gene: NPY

Linked Data

• COSMIC: COSN21545573

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285179_24285180insT , CM000669.2:g.24285179_24285180insT	GRCh38
NC_000007.13:g.24324798_24324799insT , CM000669.1:g.24324798_24324799insT	GRCh37
NC_000007.12:g.24291323_24291324insT	NCBI36
NG_016148.1:g.5992_5993insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-62_1-61insT MANE Select	ENSP00000242152.2:n.1-62_1-61insT
ENST00000242152.6:c.1-62_1-61insT	ENSP00000242152.2:n.1-62_1-61insT
ENST00000405982.1:c.-62_-61insT	ENSP00000385282.1:n.-62_-61insT
ENST00000407573.5:c.1-62_1-61insT	ENSP00000384364.1:n.1-62_1-61insT
NM_000905.3:c.1-62_1-61insT	NP_000896.1:n.1-62_1-61insT
XM_017012910.1:c.42-29481_42-29480insA	XP_016868399.1:n.42-29481_42-29480insA
XM_017012911.1:c.42-29481_42-29480insA	XP_016868400.1:n.42-29481_42-29480insA
XR_001745121.1:n.473+34177_473+34178insA
XR_001745122.1:n.345-88151_345-88150insA
XR_001745123.1:n.473+34177_473+34178insA
XR_001745124.1:n.473+34177_473+34178insA
XR_001745125.1:n.473+34177_473+34178insA
XR_001745126.1:n.473+34177_473+34178insA
XR_001745127.1:n.345-29481_345-29480insA
XR_001745129.1:n.473+34177_473+34178insA
XR_001745130.1:n.473+34177_473+34178insA
XR_001745131.1:n.473+34177_473+34178insA
XR_001745132.1:n.473+34177_473+34178insA
NM_000905.4:c.1-62_1-61insT MANE Select	NP_000896.1:n.1-62_1-61insT