Canonical Allele Identifier: CA2698501408

Gene: MYCN

Linked Data

• ClinVar Variation Id: 3062271
• ClinVar RCV Id: RCV003985993
• dbSNP Id: rs1662848905

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945739del , CM000664.2:g.15945739del	GRCh38
NC_000002.11:g.16085861del , CM000664.1:g.16085861del	GRCh37
NC_000002.10:g.16003312del	NCBI36
NG_007457.1:g.10179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.386del
ENST00000281043.4:c.1037del MANE Select	ENSP00000281043.3:p.Pro346HisfsTer5
ENST00000638417.1:c.404del	ENSP00000491476.1:p.Pro135HisfsTer5
ENST00000281043.3:c.1037del	ENSP00000281043.3:p.Pro346HisfsTer5
NM_001293228.1:c.1037del	NP_001280157.1:p.Pro346HisfsTer5
NM_001293231.1:c.404del	NP_001280160.1:p.Pro135HisfsTer5
NM_001293233.1:c.*972del	NP_001280162.1:n.*972del
NM_005378.5:c.1037del	NP_005369.2:p.Pro346HisfsTer5
NM_005378.6:c.1037del MANE Select	NP_005369.2:p.Pro346HisfsTer5
NM_001293228.2:c.1037del	NP_001280157.1:p.Pro346HisfsTer5
NM_001293231.2:c.404del	NP_001280160.1:p.Pro135HisfsTer5
NM_001293233.2:c.*972del	NP_001280162.1:n.*972del