Canonical Allele Identifier: CA2491131067

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945543_15945555delinsACTGTGGAGAAGC , CM000664.2:g.15945543_15945555delinsACTGTGGAGAAGC	GRCh38
NC_000002.11:g.16085665_16085677delinsACTGTGGAGAAGC , CM000664.1:g.16085665_16085677delinsACTGTGGAGAAGC	GRCh37
NC_000002.10:g.16003116_16003128delinsACTGTGGAGAAGC	NCBI36
NG_007457.1:g.9983_9995delinsACTGTGGAGAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.190_202delinsACTGTGGAGAAGC
ENST00000281043.4:c.841_853delinsACTGTGGAGAAGC MANE Select	ENSP00000281043.3:p.Thr281=
ENST00000638417.1:c.208_220delinsACTGTGGAGAAGC	ENSP00000491476.1:p.Thr70=
ENST00000281043.3:c.841_853delinsACTGTGGAGAAGC	ENSP00000281043.3:p.Thr281=
NM_001293228.1:c.841_853delinsACTGTGGAGAAGC	NP_001280157.1:p.Thr281=
NM_001293231.1:c.208_220delinsACTGTGGAGAAGC	NP_001280160.1:p.Thr70=
NM_001293233.1:c.*776_*788delinsACTGTGGAGAAGC	NP_001280162.1:n.*776_*788delinsACTGTGGAGAAGC
NM_005378.5:c.841_853delinsACTGTGGAGAAGC	NP_005369.2:p.Thr281=
NM_005378.6:c.841_853delinsACTGTGGAGAAGC MANE Select	NP_005369.2:p.Thr281=
NM_001293228.2:c.841_853delinsACTGTGGAGAAGC	NP_001280157.1:p.Thr281=
NM_001293231.2:c.208_220delinsACTGTGGAGAAGC	NP_001280160.1:p.Thr70=
NM_001293233.2:c.*776_*788delinsACTGTGGAGAAGC	NP_001280162.1:n.*776_*788delinsACTGTGGAGAAGC