Canonical Allele Identifier: CA2491129200

Gene: MYCN MYCNOS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942103C= , CM000664.2:g.15942103C=	GRCh38
NC_000002.11:g.16082225C= , CM000664.1:g.16082225C=	GRCh37
NC_000002.10:g.15999676C=	NCBI36
NG_007457.1:g.6543C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281043.4:c.39C= (MYCN) MANE Select	ENSP00000281043.3:p.Ile13=
ENST00000638417.1:c.157+1360C= (MYCN)	ENSP00000491476.1:n.157+1360C=
ENST00000281043.3:c.39C= (MYCN)	ENSP00000281043.3:p.Ile13=
NM_001293228.1:c.39C= (MYCN)	NP_001280157.1:p.Ile13=
NM_001293231.1:c.157+1360C= (MYCN)	NP_001280160.1:n.157+1360C=
NM_001293233.1:c.313C= (MYCN)	NP_001280162.1:p.Leu105=
NM_005378.5:c.39C= (MYCN)	NP_005369.2:p.Ile13=
NM_001329968.1:c.-234+49G= (MYCNOS)	NP_001316897.1:n.-234+49G=
XM_024452528.1:c.-234+279G= (MYCNOS)	XP_024308296.1:n.-234+279G=
NM_005378.6:c.39C= (MYCN) MANE Select	NP_005369.2:p.Ile13=
NM_001293228.2:c.39C= (MYCN)	NP_001280157.1:p.Ile13=
NM_001293231.2:c.157+1360C= (MYCN)	NP_001280160.1:n.157+1360C=
NM_001293233.2:c.313C= (MYCN)	NP_001280162.1:p.Leu105=
NR_161163.1:n.282+49G= (MYCNOS)