Canonical Allele Identifier: CA2698672352

Gene: MYCN

Linked Data

• dbSNP Id: rs2103331695

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945921del , CM000664.2:g.15945921del	GRCh38
NC_000002.11:g.16086043del , CM000664.1:g.16086043del	GRCh37
NC_000002.10:g.16003494del	NCBI36
NG_007457.1:g.10361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.568del
ENST00000281043.4:c.1219del MANE Select	ENSP00000281043.3:p.His407ThrfsTer6
ENST00000638417.1:c.586del	ENSP00000491476.1:p.His196ThrfsTer6
ENST00000281043.3:c.1219del	ENSP00000281043.3:p.His407ThrfsTer6
NM_001293228.1:c.1219del	NP_001280157.1:p.His407ThrfsTer6
NM_001293231.1:c.586del	NP_001280160.1:p.His196ThrfsTer6
NM_001293233.1:c.*1154del	NP_001280162.1:n.*1154del
NM_005378.5:c.1219del	NP_005369.2:p.His407ThrfsTer6
NM_005378.6:c.1219del MANE Select	NP_005369.2:p.His407ThrfsTer6
NM_001293228.2:c.1219del	NP_001280157.1:p.His407ThrfsTer6
NM_001293231.2:c.586del	NP_001280160.1:p.His196ThrfsTer6
NM_001293233.2:c.*1154del	NP_001280162.1:n.*1154del