Canonical Allele Identifier: CA2491129254

Gene: MYCN MYCNOS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942202G= , CM000664.2:g.15942202G=	GRCh38
NC_000002.11:g.16082324G= , CM000664.1:g.16082324G=	GRCh37
NC_000002.10:g.15999775G=	NCBI36
NG_007457.1:g.6642G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281043.4:c.138G= (MYCN) MANE Select	ENSP00000281043.3:p.Gly46=
ENST00000638417.1:c.157+1459G= (MYCN)	ENSP00000491476.1:n.157+1459G=
ENST00000281043.3:c.138G= (MYCN)	ENSP00000281043.3:p.Gly46=
NM_001293228.1:c.138G= (MYCN)	NP_001280157.1:p.Gly46=
NM_001293231.1:c.157+1459G= (MYCN)	NP_001280160.1:n.157+1459G=
NM_001293233.1:c.*73G= (MYCN)	NP_001280162.1:n.*73G=
NM_005378.5:c.138G= (MYCN)	NP_005369.2:p.Gly46=
NM_001329968.1:c.-284C= (MYCNOS)	NP_001316897.1:n.-284C=
XM_024452528.1:c.-234+180C= (MYCNOS)	XP_024308296.1:n.-234+180C=
NM_005378.6:c.138G= (MYCN) MANE Select	NP_005369.2:p.Gly46=
NM_001293228.2:c.138G= (MYCN)	NP_001280157.1:p.Gly46=
NM_001293231.2:c.157+1459G= (MYCN)	NP_001280160.1:n.157+1459G=
NM_001293233.2:c.*73G= (MYCN)	NP_001280162.1:n.*73G=
NR_161163.1:n.232C= (MYCNOS)