Canonical Allele Identifier: CA425092522

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085751T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945629T>C , CM000664.2:g.15945629T>C	GRCh38
NC_000002.11:g.16085751T>C , CM000664.1:g.16085751T>C	GRCh37
NC_000002.10:g.16003202T>C	NCBI36
NG_007457.1:g.10069T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.276T>C
ENST00000281043.4:c.927T>C MANE Select	ENSP00000281043.3:p.Gly309=
ENST00000638417.1:c.294T>C	ENSP00000491476.1:p.Gly98=
ENST00000281043.3:c.927T>C	ENSP00000281043.3:p.Gly309=
NM_001293228.1:c.927T>C	NP_001280157.1:p.Gly309=
NM_001293231.1:c.294T>C	NP_001280160.1:p.Gly98=
NM_001293233.1:c.*862T>C	NP_001280162.1:n.*862T>C
NM_005378.5:c.927T>C	NP_005369.2:p.Gly309=
NM_005378.6:c.927T>C MANE Select	NP_005369.2:p.Gly309=
NM_001293228.2:c.927T>C	NP_001280157.1:p.Gly309=
NM_001293231.2:c.294T>C	NP_001280160.1:p.Gly98=
NM_001293233.2:c.*862T>C	NP_001280162.1:n.*862T>C