Canonical Allele Identifier: CA2586968716

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945538_15945539dup , CM000664.2:g.15945538_15945539dup	GRCh38
NC_000002.11:g.16085660_16085661dup , CM000664.1:g.16085660_16085661dup	GRCh37
NC_000002.10:g.16003111_16003112dup	NCBI36
NG_007457.1:g.9978_9979dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.185_186dup
ENST00000281043.4:c.836_837dup MANE Select	ENSP00000281043.3:p.Val280TrpfsTer?
ENST00000638417.1:c.203_204dup	ENSP00000491476.1:p.Val69TrpfsTer?
ENST00000281043.3:c.836_837dup	ENSP00000281043.3:p.Val280TrpfsTer?
NM_001293228.1:c.836_837dup	NP_001280157.1:p.Val280TrpfsTer?
NM_001293231.1:c.203_204dup	NP_001280160.1:p.Val69TrpfsTer?
NM_001293233.1:c.*771_*772dup	NP_001280162.1:n.*771_*772dup
NM_005378.5:c.836_837dup	NP_005369.2:p.Val280TrpfsTer?
NM_005378.6:c.836_837dup MANE Select	NP_005369.2:p.Val280TrpfsTer?
NM_001293228.2:c.836_837dup	NP_001280157.1:p.Val280TrpfsTer?
NM_001293231.2:c.203_204dup	NP_001280160.1:p.Val69TrpfsTer?
NM_001293233.2:c.*771_*772dup	NP_001280162.1:n.*771_*772dup