Canonical Allele Identifier: CA2586968719

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945628_15945629dup , CM000664.2:g.15945628_15945629dup	GRCh38
NC_000002.11:g.16085750_16085751dup , CM000664.1:g.16085750_16085751dup	GRCh37
NC_000002.10:g.16003201_16003202dup	NCBI36
NG_007457.1:g.10068_10069dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.275_276dup
ENST00000281043.4:c.926_927dup MANE Select	ENSP00000281043.3:p.Pro310ValfsTer10
ENST00000638417.1:c.293_294dup	ENSP00000491476.1:p.Pro99ValfsTer10
ENST00000281043.3:c.926_927dup	ENSP00000281043.3:p.Pro310ValfsTer10
NM_001293228.1:c.926_927dup	NP_001280157.1:p.Pro310ValfsTer10
NM_001293231.1:c.293_294dup	NP_001280160.1:p.Pro99ValfsTer10
NM_001293233.1:c.*861_*862dup	NP_001280162.1:n.*861_*862dup
NM_005378.5:c.926_927dup	NP_005369.2:p.Pro310ValfsTer10
NM_005378.6:c.926_927dup MANE Select	NP_005369.2:p.Pro310ValfsTer10
NM_001293228.2:c.926_927dup	NP_001280157.1:p.Pro310ValfsTer10
NM_001293231.2:c.293_294dup	NP_001280160.1:p.Pro99ValfsTer10
NM_001293233.2:c.*861_*862dup	NP_001280162.1:n.*861_*862dup