Canonical Allele Identifier: CA759588182

Gene: MYCN

Linked Data

• dbSNP Id: rs1229088704
• MyVariant Identifiers: chr2:g.16085641_16085646del (hg19) ; chr2:g.15945519_15945524del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945524_15945529del , CM000664.2:g.15945524_15945529del	GRCh38
NC_000002.11:g.16085646_16085651del , CM000664.1:g.16085646_16085651del	GRCh37
NC_000002.10:g.16003097_16003102del	NCBI36
NG_007457.1:g.9964_9969del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.171_176del
ENST00000281043.4:c.822_827del MANE Select	ENSP00000281043.3:p.Glu275_Glu276del
ENST00000638417.1:c.189_194del	ENSP00000491476.1:p.Glu64_Glu65del
ENST00000281043.3:c.822_827del	ENSP00000281043.3:p.Glu275_Glu276del
NM_001293228.1:c.822_827del	NP_001280157.1:p.Glu275_Glu276del
NM_001293231.1:c.189_194del	NP_001280160.1:p.Glu64_Glu65del
NM_001293233.1:c.*757_*762del	NP_001280162.1:n.*757_*762del
NM_005378.5:c.822_827del	NP_005369.2:p.Glu275_Glu276del
NM_005378.6:c.822_827del MANE Select	NP_005369.2:p.Glu275_Glu276del
NM_001293228.2:c.822_827del	NP_001280157.1:p.Glu275_Glu276del
NM_001293231.2:c.189_194del	NP_001280160.1:p.Glu64_Glu65del
NM_001293233.2:c.*757_*762del	NP_001280162.1:n.*757_*762del