Canonical Allele Identifier: CA2491131089

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945585A= , CM000664.2:g.15945585A=	GRCh38
NC_000002.11:g.16085707A= , CM000664.1:g.16085707A=	GRCh37
NC_000002.10:g.16003158A=	NCBI36
NG_007457.1:g.10025A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.232A=
ENST00000281043.4:c.883A= MANE Select	ENSP00000281043.3:p.Thr295=
ENST00000638417.1:c.250A=	ENSP00000491476.1:p.Thr84=
ENST00000281043.3:c.883A=	ENSP00000281043.3:p.Thr295=
NM_001293228.1:c.883A=	NP_001280157.1:p.Thr295=
NM_001293231.1:c.250A=	NP_001280160.1:p.Thr84=
NM_001293233.1:c.*818A=	NP_001280162.1:n.*818A=
NM_005378.5:c.883A=	NP_005369.2:p.Thr295=
NM_005378.6:c.883A= MANE Select	NP_005369.2:p.Thr295=
NM_001293228.2:c.883A=	NP_001280157.1:p.Thr295=
NM_001293231.2:c.250A=	NP_001280160.1:p.Thr84=
NM_001293233.2:c.*818A=	NP_001280162.1:n.*818A=