Canonical Allele Identifier: CA425056976

Gene: MYCN

Linked Data

• dbSNP Id: rs1662838773
• gnomAD v3: 2-15945518-TGAA-T
• gnomAD v4: 2-15945518-TGAA-T
• MyVariant Identifiers: chr2:g.16085641_16085643del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945521_15945523del , CM000664.2:g.15945521_15945523del	GRCh38
NC_000002.11:g.16085643_16085645del , CM000664.1:g.16085643_16085645del	GRCh37
NC_000002.10:g.16003094_16003096del	NCBI36
NG_007457.1:g.9961_9963del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.168_170del
ENST00000281043.4:c.819_821del MANE Select	ENSP00000281043.3:p.Glu274del
ENST00000638417.1:c.186_188del	ENSP00000491476.1:p.Glu63del
ENST00000281043.3:c.819_821del	ENSP00000281043.3:p.Glu274del
NM_001293228.1:c.819_821del	NP_001280157.1:p.Glu274del
NM_001293231.1:c.186_188del	NP_001280160.1:p.Glu63del
NM_001293233.1:c.*754_*756del	NP_001280162.1:n.*754_*756del
NM_005378.5:c.819_821del	NP_005369.2:p.Glu274del
NM_005378.6:c.819_821del MANE Select	NP_005369.2:p.Glu274del
NM_001293228.2:c.819_821del	NP_001280157.1:p.Glu274del
NM_001293231.2:c.186_188del	NP_001280160.1:p.Glu63del
NM_001293233.2:c.*754_*756del	NP_001280162.1:n.*754_*756del