Canonical Allele Identifier: CA2657954663

Gene: MYCN

Linked Data

• gnomAD v4: 2-15945878-GCGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945882_15945884del , CM000664.2:g.15945882_15945884del	GRCh38
NC_000002.11:g.16086004_16086006del , CM000664.1:g.16086004_16086006del	GRCh37
NC_000002.10:g.16003455_16003457del	NCBI36
NG_007457.1:g.10322_10324del

Transcript Alleles

HGVS	Amino-acid change
ENST00000703162.1:n.529_531del
ENST00000281043.4:c.1180_1182del MANE Select	ENSP00000281043.3:p.Arg394del
ENST00000638417.1:c.547_549del	ENSP00000491476.1:p.Arg183del
ENST00000281043.3:c.1180_1182del	ENSP00000281043.3:p.Arg394del
NM_001293228.1:c.1180_1182del	NP_001280157.1:p.Arg394del
NM_001293231.1:c.547_549del	NP_001280160.1:p.Arg183del
NM_001293233.1:c.*1115_*1117del	NP_001280162.1:n.*1115_*1117del
NM_005378.5:c.1180_1182del	NP_005369.2:p.Arg394del
NM_005378.6:c.1180_1182del MANE Select	NP_005369.2:p.Arg394del
NM_001293228.2:c.1180_1182del	NP_001280157.1:p.Arg394del
NM_001293231.2:c.547_549del	NP_001280160.1:p.Arg183del
NM_001293233.2:c.*1115_*1117del	NP_001280162.1:n.*1115_*1117del