Canonical Allele Identifier: CA2491131050

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945512_15945518delinsGGAAGAT , CM000664.2:g.15945512_15945518delinsGGAAGAT	GRCh38
NC_000002.11:g.16085634_16085640delinsGGAAGAT , CM000664.1:g.16085634_16085640delinsGGAAGAT	GRCh37
NC_000002.10:g.16003085_16003091delinsGGAAGAT	NCBI36
NG_007457.1:g.9952_9958delinsGGAAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.159_165delinsGGAAGAT
ENST00000281043.4:c.810_816delinsGGAAGAT MANE Select	ENSP00000281043.3:p.Glu270=
ENST00000638417.1:c.177_183delinsGGAAGAT	ENSP00000491476.1:p.Glu59=
ENST00000281043.3:c.810_816delinsGGAAGAT	ENSP00000281043.3:p.Glu270=
NM_001293228.1:c.810_816delinsGGAAGAT	NP_001280157.1:p.Glu270=
NM_001293231.1:c.177_183delinsGGAAGAT	NP_001280160.1:p.Glu59=
NM_001293233.1:c.*745_*751delinsGGAAGAT	NP_001280162.1:n.*745_*751delinsGGAAGAT
NM_005378.5:c.810_816delinsGGAAGAT	NP_005369.2:p.Glu270=
NM_005378.6:c.810_816delinsGGAAGAT MANE Select	NP_005369.2:p.Glu270=
NM_001293228.2:c.810_816delinsGGAAGAT	NP_001280157.1:p.Glu270=
NM_001293231.2:c.177_183delinsGGAAGAT	NP_001280160.1:p.Glu59=
NM_001293233.2:c.*745_*751delinsGGAAGAT	NP_001280162.1:n.*745_*751delinsGGAAGAT