Canonical Allele Identifier: CA1027884720

Gene: MYCN

Linked Data

• gnomAD v3: 2-15945555-C-CG
• gnomAD v4: 2-15945555-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945557dup , CM000664.2:g.15945557dup	GRCh38
NC_000002.11:g.16085679dup , CM000664.1:g.16085679dup	GRCh37
NC_000002.10:g.16003130dup	NCBI36
NG_007457.1:g.9997dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.204dup
ENST00000281043.4:c.855dup MANE Select	ENSP00000281043.3:p.Arg286AlafsTer?
ENST00000638417.1:c.222dup	ENSP00000491476.1:p.Arg75AlafsTer?
ENST00000281043.3:c.855dup	ENSP00000281043.3:p.Arg286AlafsTer?
NM_001293228.1:c.855dup	NP_001280157.1:p.Arg286AlafsTer?
NM_001293231.1:c.222dup	NP_001280160.1:p.Arg75AlafsTer?
NM_001293233.1:c.*790dup	NP_001280162.1:n.*790dup
NM_005378.5:c.855dup	NP_005369.2:p.Arg286AlafsTer?
NM_005378.6:c.855dup MANE Select	NP_005369.2:p.Arg286AlafsTer?
NM_001293228.2:c.855dup	NP_001280157.1:p.Arg286AlafsTer?
NM_001293231.2:c.222dup	NP_001280160.1:p.Arg75AlafsTer?
NM_001293233.2:c.*790dup	NP_001280162.1:n.*790dup