Canonical Allele Identifier: CA2491131100

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945601_15945603delinsCTG , CM000664.2:g.15945601_15945603delinsCTG	GRCh38
NC_000002.11:g.16085723_16085725delinsCTG , CM000664.1:g.16085723_16085725delinsCTG	GRCh37
NC_000002.10:g.16003174_16003176delinsCTG	NCBI36
NG_007457.1:g.10041_10043delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.248_250delinsCTG
ENST00000281043.4:c.899_901delinsCTG MANE Select	ENSP00000281043.3:p.Thr300=
ENST00000638417.1:c.266_268delinsCTG	ENSP00000491476.1:p.Thr89=
ENST00000281043.3:c.899_901delinsCTG	ENSP00000281043.3:p.Thr300=
NM_001293228.1:c.899_901delinsCTG	NP_001280157.1:p.Thr300=
NM_001293231.1:c.266_268delinsCTG	NP_001280160.1:p.Thr89=
NM_001293233.1:c.*834_*836delinsCTG	NP_001280162.1:n.*834_*836delinsCTG
NM_005378.5:c.899_901delinsCTG	NP_005369.2:p.Thr300=
NM_005378.6:c.899_901delinsCTG MANE Select	NP_005369.2:p.Thr300=
NM_001293228.2:c.899_901delinsCTG	NP_001280157.1:p.Thr300=
NM_001293231.2:c.266_268delinsCTG	NP_001280160.1:p.Thr89=
NM_001293233.2:c.*834_*836delinsCTG	NP_001280162.1:n.*834_*836delinsCTG