Canonical Allele Identifier: CA2682048138

Gene: NPY

Linked Data

• gnomAD v4: 7-24285130-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285130_24285131insA , CM000669.2:g.24285130_24285131insA	GRCh38
NC_000007.13:g.24324749_24324750insA , CM000669.1:g.24324749_24324750insA	GRCh37
NC_000007.12:g.24291274_24291275insA	NCBI36
NG_016148.1:g.5943_5944insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-111_1-110insA MANE Select	ENSP00000242152.2:n.1-111_1-110insA
ENST00000242152.6:c.1-111_1-110insA	ENSP00000242152.2:n.1-111_1-110insA
ENST00000405982.1:c.-111_-110insA	ENSP00000385282.1:n.-111_-110insA
ENST00000407573.5:c.-1+54_-1+55insA	ENSP00000384364.1:n.-1+54_-1+55insA
NM_000905.3:c.1-111_1-110insA	NP_000896.1:n.1-111_1-110insA
XM_017012910.1:c.42-29432_42-29431insT	XP_016868399.1:n.42-29432_42-29431insT
XM_017012911.1:c.42-29432_42-29431insT	XP_016868400.1:n.42-29432_42-29431insT
XR_001745121.1:n.473+34226_473+34227insT
XR_001745122.1:n.345-88102_345-88101insT
XR_001745123.1:n.473+34226_473+34227insT
XR_001745124.1:n.473+34226_473+34227insT
XR_001745125.1:n.473+34226_473+34227insT
XR_001745126.1:n.473+34226_473+34227insT
XR_001745127.1:n.345-29432_345-29431insT
XR_001745129.1:n.473+34226_473+34227insT
XR_001745130.1:n.473+34226_473+34227insT
XR_001745131.1:n.473+34226_473+34227insT
XR_001745132.1:n.473+34226_473+34227insT
NM_000905.4:c.1-111_1-110insA MANE Select	NP_000896.1:n.1-111_1-110insA