Canonical Allele Identifier: CA2491131024

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945466_15945470delinsTGAGA , CM000664.2:g.15945466_15945470delinsTGAGA	GRCh38
NC_000002.11:g.16085588_16085592delinsTGAGA , CM000664.1:g.16085588_16085592delinsTGAGA	GRCh37
NC_000002.10:g.16003039_16003043delinsTGAGA	NCBI36
NG_007457.1:g.9906_9910delinsTGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-27_140-23delinsTGAGA
ENST00000281043.4:c.791-27_791-23delinsTGAGA MANE Select	ENSP00000281043.3:n.791-27_791-23delinsTGAGA
ENST00000638417.1:c.158-27_158-23delinsTGAGA	ENSP00000491476.1:n.158-27_158-23delinsTGAGA
ENST00000281043.3:c.791-27_791-23delinsTGAGA	ENSP00000281043.3:n.791-27_791-23delinsTGAGA
NM_001293228.1:c.791-27_791-23delinsTGAGA	NP_001280157.1:n.791-27_791-23delinsTGAGA
NM_001293231.1:c.158-27_158-23delinsTGAGA	NP_001280160.1:n.158-27_158-23delinsTGAGA
NM_001293233.1:c.*726-27_*726-23delinsTGAGA	NP_001280162.1:n.*726-27_*726-23delinsTGAGA
NM_005378.5:c.791-27_791-23delinsTGAGA	NP_005369.2:n.791-27_791-23delinsTGAGA
NM_005378.6:c.791-27_791-23delinsTGAGA MANE Select	NP_005369.2:n.791-27_791-23delinsTGAGA
NM_001293228.2:c.791-27_791-23delinsTGAGA	NP_001280157.1:n.791-27_791-23delinsTGAGA
NM_001293231.2:c.158-27_158-23delinsTGAGA	NP_001280160.1:n.158-27_158-23delinsTGAGA
NM_001293233.2:c.*726-27_*726-23delinsTGAGA	NP_001280162.1:n.*726-27_*726-23delinsTGAGA