Canonical Allele Identifier: CA2491131096

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945596C= , CM000664.2:g.15945596C=	GRCh38
NC_000002.11:g.16085718C= , CM000664.1:g.16085718C=	GRCh37
NC_000002.10:g.16003169C=	NCBI36
NG_007457.1:g.10036C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.243C=
ENST00000281043.4:c.894C= MANE Select	ENSP00000281043.3:p.Thr298=
ENST00000638417.1:c.261C=	ENSP00000491476.1:p.Thr87=
ENST00000281043.3:c.894C=	ENSP00000281043.3:p.Thr298=
NM_001293228.1:c.894C=	NP_001280157.1:p.Thr298=
NM_001293231.1:c.261C=	NP_001280160.1:p.Thr87=
NM_001293233.1:c.*829C=	NP_001280162.1:n.*829C=
NM_005378.5:c.894C=	NP_005369.2:p.Thr298=
NM_005378.6:c.894C= MANE Select	NP_005369.2:p.Thr298=
NM_001293228.2:c.894C=	NP_001280157.1:p.Thr298=
NM_001293231.2:c.261C=	NP_001280160.1:p.Thr87=
NM_001293233.2:c.*829C=	NP_001280162.1:n.*829C=