Canonical Allele Identifier: CA345931826

Gene: MYCN

Linked Data

• gnomAD v4: 2-15945591-T-C
• MyVariant Identifiers: chr2:g.16085713T>C (hg19) ; chr2:g.15945591T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945591T>C , CM000664.2:g.15945591T>C	GRCh38
NC_000002.11:g.16085713T>C , CM000664.1:g.16085713T>C	GRCh37
NC_000002.10:g.16003164T>C	NCBI36
NG_007457.1:g.10031T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.238T>C
ENST00000281043.4:c.889T>C MANE Select	ENSP00000281043.3:p.Phe297Leu
ENST00000638417.1:c.256T>C	ENSP00000491476.1:p.Phe86Leu
ENST00000281043.3:c.889T>C	ENSP00000281043.3:p.Phe297Leu
NM_001293228.1:c.889T>C	NP_001280157.1:p.Phe297Leu
NM_001293231.1:c.256T>C	NP_001280160.1:p.Phe86Leu
NM_001293233.1:c.*824T>C	NP_001280162.1:n.*824T>C
NM_005378.5:c.889T>C	NP_005369.2:p.Phe297Leu
NM_005378.6:c.889T>C MANE Select	NP_005369.2:p.Phe297Leu
NM_001293228.2:c.889T>C	NP_001280157.1:p.Phe297Leu
NM_001293231.2:c.256T>C	NP_001280160.1:p.Phe86Leu
NM_001293233.2:c.*824T>C	NP_001280162.1:n.*824T>C