Canonical Allele Identifier: CA2695202168

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945705_15945706delinsTT , CM000664.2:g.15945705_15945706delinsTT	GRCh38
NC_000002.11:g.16085827_16085828delinsTT , CM000664.1:g.16085827_16085828delinsTT	GRCh37
NC_000002.10:g.16003278_16003279delinsTT	NCBI36
NG_007457.1:g.10145_10146delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.352_353delinsTT
ENST00000281043.4:c.1003_1004delinsTT MANE Select	ENSP00000281043.3:p.Pro335Phe
ENST00000638417.1:c.370_371delinsTT	ENSP00000491476.1:p.Pro124Phe
ENST00000281043.3:c.1003_1004delinsTT	ENSP00000281043.3:p.Pro335Phe
NM_001293228.1:c.1003_1004delinsTT	NP_001280157.1:p.Pro335Phe
NM_001293231.1:c.370_371delinsTT	NP_001280160.1:p.Pro124Phe
NM_001293233.1:c.*938_*939delinsTT	NP_001280162.1:n.*938_*939delinsTT
NM_005378.5:c.1003_1004delinsTT	NP_005369.2:p.Pro335Phe
NM_005378.6:c.1003_1004delinsTT MANE Select	NP_005369.2:p.Pro335Phe
NM_001293228.2:c.1003_1004delinsTT	NP_001280157.1:p.Pro335Phe
NM_001293231.2:c.370_371delinsTT	NP_001280160.1:p.Pro124Phe
NM_001293233.2:c.*938_*939delinsTT	NP_001280162.1:n.*938_*939delinsTT