Canonical Allele Identifier: CA2657954656

Gene: MYCN

Linked Data

• gnomAD v4: 2-15945838-A-ACAGTGAGCGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945840_15945849dup , CM000664.2:g.15945840_15945849dup	GRCh38
NC_000002.11:g.16085962_16085971dup , CM000664.1:g.16085962_16085971dup	GRCh37
NC_000002.10:g.16003413_16003422dup	NCBI36
NG_007457.1:g.10280_10289dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000703162.1:n.487_496dup
ENST00000281043.4:c.1138_1147dup MANE Select	ENSP00000281043.3:p.Arg383GlnfsTer2
ENST00000638417.1:c.505_514dup	ENSP00000491476.1:p.Arg172GlnfsTer2
ENST00000281043.3:c.1138_1147dup	ENSP00000281043.3:p.Arg383GlnfsTer2
NM_001293228.1:c.1138_1147dup	NP_001280157.1:p.Arg383GlnfsTer2
NM_001293231.1:c.505_514dup	NP_001280160.1:p.Arg172GlnfsTer2
NM_001293233.1:c.*1073_*1082dup	NP_001280162.1:n.*1073_*1082dup
NM_005378.5:c.1138_1147dup	NP_005369.2:p.Arg383GlnfsTer2
NM_005378.6:c.1138_1147dup MANE Select	NP_005369.2:p.Arg383GlnfsTer2
NM_001293228.2:c.1138_1147dup	NP_001280157.1:p.Arg383GlnfsTer2
NM_001293231.2:c.505_514dup	NP_001280160.1:p.Arg172GlnfsTer2
NM_001293233.2:c.*1073_*1082dup	NP_001280162.1:n.*1073_*1082dup