Canonical Allele Identifier: CA425056949

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085616T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945494T>C , CM000664.2:g.15945494T>C	GRCh38
NC_000002.11:g.16085616T>C , CM000664.1:g.16085616T>C	GRCh37
NC_000002.10:g.16003067T>C	NCBI36
NG_007457.1:g.9934T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.141T>C
ENST00000281043.4:c.792T>C MANE Select	ENSP00000281043.3:p.Asp264=
ENST00000638417.1:c.159T>C	ENSP00000491476.1:p.Asp53=
ENST00000281043.3:c.792T>C	ENSP00000281043.3:p.Asp264=
NM_001293228.1:c.792T>C	NP_001280157.1:p.Asp264=
NM_001293231.1:c.159T>C	NP_001280160.1:p.Asp53=
NM_001293233.1:c.*727T>C	NP_001280162.1:n.*727T>C
NM_005378.5:c.792T>C	NP_005369.2:p.Asp264=
NM_005378.6:c.792T>C MANE Select	NP_005369.2:p.Asp264=
NM_001293228.2:c.792T>C	NP_001280157.1:p.Asp264=
NM_001293231.2:c.159T>C	NP_001280160.1:p.Asp53=
NM_001293233.2:c.*727T>C	NP_001280162.1:n.*727T>C