Canonical Allele Identifier: CA2491131068

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945544_15945546delinsCTG , CM000664.2:g.15945544_15945546delinsCTG	GRCh38
NC_000002.11:g.16085666_16085668delinsCTG , CM000664.1:g.16085666_16085668delinsCTG	GRCh37
NC_000002.10:g.16003117_16003119delinsCTG	NCBI36
NG_007457.1:g.9984_9986delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.191_193delinsCTG
ENST00000281043.4:c.842_844delinsCTG MANE Select	ENSP00000281043.3:p.Thr281=
ENST00000638417.1:c.209_211delinsCTG	ENSP00000491476.1:p.Thr70=
ENST00000281043.3:c.842_844delinsCTG	ENSP00000281043.3:p.Thr281=
NM_001293228.1:c.842_844delinsCTG	NP_001280157.1:p.Thr281=
NM_001293231.1:c.209_211delinsCTG	NP_001280160.1:p.Thr70=
NM_001293233.1:c.*777_*779delinsCTG	NP_001280162.1:n.*777_*779delinsCTG
NM_005378.5:c.842_844delinsCTG	NP_005369.2:p.Thr281=
NM_005378.6:c.842_844delinsCTG MANE Select	NP_005369.2:p.Thr281=
NM_001293228.2:c.842_844delinsCTG	NP_001280157.1:p.Thr281=
NM_001293231.2:c.209_211delinsCTG	NP_001280160.1:p.Thr70=
NM_001293233.2:c.*777_*779delinsCTG	NP_001280162.1:n.*777_*779delinsCTG