Canonical Allele Identifier: CA2576682129

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945880_15945892dup , CM000664.2:g.15945880_15945892dup	GRCh38
NC_000002.11:g.16086002_16086014dup , CM000664.1:g.16086002_16086014dup	GRCh37
NC_000002.10:g.16003453_16003465dup	NCBI36
NG_007457.1:g.10320_10332dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000703162.1:n.527_539dup
ENST00000281043.4:c.1178_1190dup MANE Select	ENSP00000281043.3:p.Arg398ProfsTer22
ENST00000638417.1:c.545_557dup	ENSP00000491476.1:p.Arg187ProfsTer22
ENST00000281043.3:c.1178_1190dup	ENSP00000281043.3:p.Arg398ProfsTer22
NM_001293228.1:c.1178_1190dup	NP_001280157.1:p.Arg398ProfsTer22
NM_001293231.1:c.545_557dup	NP_001280160.1:p.Arg187ProfsTer22
NM_001293233.1:c.*1113_*1125dup	NP_001280162.1:n.*1113_*1125dup
NM_005378.5:c.1178_1190dup	NP_005369.2:p.Arg398ProfsTer22
NM_005378.6:c.1178_1190dup MANE Select	NP_005369.2:p.Arg398ProfsTer22
NM_001293228.2:c.1178_1190dup	NP_001280157.1:p.Arg398ProfsTer22
NM_001293231.2:c.545_557dup	NP_001280160.1:p.Arg187ProfsTer22
NM_001293233.2:c.*1113_*1125dup	NP_001280162.1:n.*1113_*1125dup