Canonical Allele Identifier: CA425056984

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085649A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945527A>G , CM000664.2:g.15945527A>G	GRCh38
NC_000002.11:g.16085649A>G , CM000664.1:g.16085649A>G	GRCh37
NC_000002.10:g.16003100A>G	NCBI36
NG_007457.1:g.9967A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.174A>G
ENST00000281043.4:c.825A>G MANE Select	ENSP00000281043.3:p.Glu275=
ENST00000638417.1:c.192A>G	ENSP00000491476.1:p.Glu64=
ENST00000281043.3:c.825A>G	ENSP00000281043.3:p.Glu275=
NM_001293228.1:c.825A>G	NP_001280157.1:p.Glu275=
NM_001293231.1:c.192A>G	NP_001280160.1:p.Glu64=
NM_001293233.1:c.*760A>G	NP_001280162.1:n.*760A>G
NM_005378.5:c.825A>G	NP_005369.2:p.Glu275=
NM_005378.6:c.825A>G MANE Select	NP_005369.2:p.Glu275=
NM_001293228.2:c.825A>G	NP_001280157.1:p.Glu275=
NM_001293231.2:c.192A>G	NP_001280160.1:p.Glu64=
NM_001293233.2:c.*760A>G	NP_001280162.1:n.*760A>G