Canonical Allele Identifier: CA2586968721

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945708del , CM000664.2:g.15945708del	GRCh38
NC_000002.11:g.16085830del , CM000664.1:g.16085830del	GRCh37
NC_000002.10:g.16003281del	NCBI36
NG_007457.1:g.10148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.355del
ENST00000281043.4:c.1006del MANE Select	ENSP00000281043.3:p.Ser336LeufsTer15
ENST00000638417.1:c.373del	ENSP00000491476.1:p.Ser125LeufsTer15
ENST00000281043.3:c.1006del	ENSP00000281043.3:p.Ser336LeufsTer15
NM_001293228.1:c.1006del	NP_001280157.1:p.Ser336LeufsTer15
NM_001293231.1:c.373del	NP_001280160.1:p.Ser125LeufsTer15
NM_001293233.1:c.*941del	NP_001280162.1:n.*941del
NM_005378.5:c.1006del	NP_005369.2:p.Ser336LeufsTer15
NM_005378.6:c.1006del MANE Select	NP_005369.2:p.Ser336LeufsTer15
NM_001293228.2:c.1006del	NP_001280157.1:p.Ser336LeufsTer15
NM_001293231.2:c.373del	NP_001280160.1:p.Ser125LeufsTer15
NM_001293233.2:c.*941del	NP_001280162.1:n.*941del