Canonical Allele Identifier: CA2491131078

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945560_15945563delinsTTCC , CM000664.2:g.15945560_15945563delinsTTCC	GRCh38
NC_000002.11:g.16085682_16085685delinsTTCC , CM000664.1:g.16085682_16085685delinsTTCC	GRCh37
NC_000002.10:g.16003133_16003136delinsTTCC	NCBI36
NG_007457.1:g.10000_10003delinsTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.207_210delinsTTCC
ENST00000281043.4:c.858_861delinsTTCC MANE Select	ENSP00000281043.3:p.Arg286=
ENST00000638417.1:c.225_228delinsTTCC	ENSP00000491476.1:p.Arg75=
ENST00000281043.3:c.858_861delinsTTCC	ENSP00000281043.3:p.Arg286=
NM_001293228.1:c.858_861delinsTTCC	NP_001280157.1:p.Arg286=
NM_001293231.1:c.225_228delinsTTCC	NP_001280160.1:p.Arg75=
NM_001293233.1:c.*793_*796delinsTTCC	NP_001280162.1:n.*793_*796delinsTTCC
NM_005378.5:c.858_861delinsTTCC	NP_005369.2:p.Arg286=
NM_005378.6:c.858_861delinsTTCC MANE Select	NP_005369.2:p.Arg286=
NM_001293228.2:c.858_861delinsTTCC	NP_001280157.1:p.Arg286=
NM_001293231.2:c.225_228delinsTTCC	NP_001280160.1:p.Arg75=
NM_001293233.2:c.*793_*796delinsTTCC	NP_001280162.1:n.*793_*796delinsTTCC