Canonical Allele Identifier: CA425092821

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085895T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945773T>C , CM000664.2:g.15945773T>C	GRCh38
NC_000002.11:g.16085895T>C , CM000664.1:g.16085895T>C	GRCh37
NC_000002.10:g.16003346T>C	NCBI36
NG_007457.1:g.10213T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.420T>C
ENST00000281043.4:c.1071T>C MANE Select	ENSP00000281043.3:p.Arg357=
ENST00000638417.1:c.438T>C	ENSP00000491476.1:p.Arg146=
ENST00000281043.3:c.1071T>C	ENSP00000281043.3:p.Arg357=
NM_001293228.1:c.1071T>C	NP_001280157.1:p.Arg357=
NM_001293231.1:c.438T>C	NP_001280160.1:p.Arg146=
NM_001293233.1:c.*1006T>C	NP_001280162.1:n.*1006T>C
NM_005378.5:c.1071T>C	NP_005369.2:p.Arg357=
NM_005378.6:c.1071T>C MANE Select	NP_005369.2:p.Arg357=
NM_001293228.2:c.1071T>C	NP_001280157.1:p.Arg357=
NM_001293231.2:c.438T>C	NP_001280160.1:p.Arg146=
NM_001293233.2:c.*1006T>C	NP_001280162.1:n.*1006T>C