Canonical Allele Identifier: CA2491131041

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945497_15945500delinsTGAA , CM000664.2:g.15945497_15945500delinsTGAA	GRCh38
NC_000002.11:g.16085619_16085622delinsTGAA , CM000664.1:g.16085619_16085622delinsTGAA	GRCh37
NC_000002.10:g.16003070_16003073delinsTGAA	NCBI36
NG_007457.1:g.9937_9940delinsTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.144_147delinsTGAA
ENST00000281043.4:c.795_798delinsTGAA MANE Select	ENSP00000281043.3:p.Asp265=
ENST00000638417.1:c.162_165delinsTGAA	ENSP00000491476.1:p.Asp54=
ENST00000281043.3:c.795_798delinsTGAA	ENSP00000281043.3:p.Asp265=
NM_001293228.1:c.795_798delinsTGAA	NP_001280157.1:p.Asp265=
NM_001293231.1:c.162_165delinsTGAA	NP_001280160.1:p.Asp54=
NM_001293233.1:c.*730_*733delinsTGAA	NP_001280162.1:n.*730_*733delinsTGAA
NM_005378.5:c.795_798delinsTGAA	NP_005369.2:p.Asp265=
NM_005378.6:c.795_798delinsTGAA MANE Select	NP_005369.2:p.Asp265=
NM_001293228.2:c.795_798delinsTGAA	NP_001280157.1:p.Asp265=
NM_001293231.2:c.162_165delinsTGAA	NP_001280160.1:p.Asp54=
NM_001293233.2:c.*730_*733delinsTGAA	NP_001280162.1:n.*730_*733delinsTGAA