Canonical Allele Identifier: CA2586968717

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945583_15945584dup , CM000664.2:g.15945583_15945584dup	GRCh38
NC_000002.11:g.16085705_16085706dup , CM000664.1:g.16085705_16085706dup	GRCh37
NC_000002.10:g.16003156_16003157dup	NCBI36
NG_007457.1:g.10023_10024dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.230_231dup
ENST00000281043.4:c.881_882dup MANE Select	ENSP00000281043.3:p.Thr295SerfsTer25
ENST00000638417.1:c.248_249dup	ENSP00000491476.1:p.Thr84SerfsTer25
ENST00000281043.3:c.881_882dup	ENSP00000281043.3:p.Thr295SerfsTer25
NM_001293228.1:c.881_882dup	NP_001280157.1:p.Thr295SerfsTer25
NM_001293231.1:c.248_249dup	NP_001280160.1:p.Thr84SerfsTer25
NM_001293233.1:c.*816_*817dup	NP_001280162.1:n.*816_*817dup
NM_005378.5:c.881_882dup	NP_005369.2:p.Thr295SerfsTer25
NM_005378.6:c.881_882dup MANE Select	NP_005369.2:p.Thr295SerfsTer25
NM_001293228.2:c.881_882dup	NP_001280157.1:p.Thr295SerfsTer25
NM_001293231.2:c.248_249dup	NP_001280160.1:p.Thr84SerfsTer25
NM_001293233.2:c.*816_*817dup	NP_001280162.1:n.*816_*817dup