Canonical Allele Identifier: CA425057124

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085724T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945602T>A , CM000664.2:g.15945602T>A	GRCh38
NC_000002.11:g.16085724T>A , CM000664.1:g.16085724T>A	GRCh37
NC_000002.10:g.16003175T>A	NCBI36
NG_007457.1:g.10042T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.249T>A
ENST00000281043.4:c.900T>A MANE Select	ENSP00000281043.3:p.Thr300=
ENST00000638417.1:c.267T>A	ENSP00000491476.1:p.Thr89=
ENST00000281043.3:c.900T>A	ENSP00000281043.3:p.Thr300=
NM_001293228.1:c.900T>A	NP_001280157.1:p.Thr300=
NM_001293231.1:c.267T>A	NP_001280160.1:p.Thr89=
NM_001293233.1:c.*835T>A	NP_001280162.1:n.*835T>A
NM_005378.5:c.900T>A	NP_005369.2:p.Thr300=
NM_005378.6:c.900T>A MANE Select	NP_005369.2:p.Thr300=
NM_001293228.2:c.900T>A	NP_001280157.1:p.Thr300=
NM_001293231.2:c.267T>A	NP_001280160.1:p.Thr89=
NM_001293233.2:c.*835T>A	NP_001280162.1:n.*835T>A