Canonical Allele Identifier: CA2491131045

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945500_15945501delinsAG , CM000664.2:g.15945500_15945501delinsAG	GRCh38
NC_000002.11:g.16085622_16085623delinsAG , CM000664.1:g.16085622_16085623delinsAG	GRCh37
NC_000002.10:g.16003073_16003074delinsAG	NCBI36
NG_007457.1:g.9940_9941delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.147_148delinsAG
ENST00000281043.4:c.798_799delinsAG MANE Select	ENSP00000281043.3:p.Glu266=
ENST00000638417.1:c.165_166delinsAG	ENSP00000491476.1:p.Glu55=
ENST00000281043.3:c.798_799delinsAG	ENSP00000281043.3:p.Glu266=
NM_001293228.1:c.798_799delinsAG	NP_001280157.1:p.Glu266=
NM_001293231.1:c.165_166delinsAG	NP_001280160.1:p.Glu55=
NM_001293233.1:c.*733_*734delinsAG	NP_001280162.1:n.*733_*734delinsAG
NM_005378.5:c.798_799delinsAG	NP_005369.2:p.Glu266=
NM_005378.6:c.798_799delinsAG MANE Select	NP_005369.2:p.Glu266=
NM_001293228.2:c.798_799delinsAG	NP_001280157.1:p.Glu266=
NM_001293231.2:c.165_166delinsAG	NP_001280160.1:p.Glu55=
NM_001293233.2:c.*733_*734delinsAG	NP_001280162.1:n.*733_*734delinsAG