Canonical Allele Identifier: CA2698689678

Gene: MYCN

Linked Data

• dbSNP Id: rs2103330402

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945540del , CM000664.2:g.15945540del	GRCh38
NC_000002.11:g.16085662del , CM000664.1:g.16085662del	GRCh37
NC_000002.10:g.16003113del	NCBI36
NG_007457.1:g.9980del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.187del
ENST00000281043.4:c.838del MANE Select	ENSP00000281043.3:p.Val280SerfsTer?
ENST00000638417.1:c.205del	ENSP00000491476.1:p.Val69SerfsTer?
ENST00000281043.3:c.838del	ENSP00000281043.3:p.Val280SerfsTer?
NM_001293228.1:c.838del	NP_001280157.1:p.Val280SerfsTer?
NM_001293231.1:c.205del	NP_001280160.1:p.Val69SerfsTer?
NM_001293233.1:c.*773del	NP_001280162.1:n.*773del
NM_005378.5:c.838del	NP_005369.2:p.Val280SerfsTer?
NM_005378.6:c.838del MANE Select	NP_005369.2:p.Val280SerfsTer?
NM_001293228.2:c.838del	NP_001280157.1:p.Val280SerfsTer?
NM_001293231.2:c.205del	NP_001280160.1:p.Val69SerfsTer?
NM_001293233.2:c.*773del	NP_001280162.1:n.*773del