Canonical Allele Identifier: CA345930020

Gene: MYCN MYCNOS

Linked Data

• MyVariant Identifiers: chr2:g.16082228C>G (hg19) ; chr2:g.15942106C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942106C>G , CM000664.2:g.15942106C>G	GRCh38
NC_000002.11:g.16082228C>G , CM000664.1:g.16082228C>G	GRCh37
NC_000002.10:g.15999679C>G	NCBI36
NG_007457.1:g.6546C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281043.4:c.42C>G (MYCN) MANE Select	ENSP00000281043.3:p.Cys14Trp
ENST00000638417.1:c.157+1363C>G (MYCN)	ENSP00000491476.1:n.157+1363C>G
ENST00000281043.3:c.42C>G (MYCN)	ENSP00000281043.3:p.Cys14Trp
NM_001293228.1:c.42C>G (MYCN)	NP_001280157.1:p.Cys14Trp
NM_001293231.1:c.157+1363C>G (MYCN)	NP_001280160.1:n.157+1363C>G
NM_001293233.1:c.316C>G (MYCN)	NP_001280162.1:p.Gln106Glu
NM_005378.5:c.42C>G (MYCN)	NP_005369.2:p.Cys14Trp
NM_001329968.1:c.-234+46G>C (MYCNOS)	NP_001316897.1:n.-234+46G>C
XM_024452528.1:c.-234+276G>C (MYCNOS)	XP_024308296.1:n.-234+276G>C
NM_005378.6:c.42C>G (MYCN) MANE Select	NP_005369.2:p.Cys14Trp
NM_001293228.2:c.42C>G (MYCN)	NP_001280157.1:p.Cys14Trp
NM_001293231.2:c.157+1363C>G (MYCN)	NP_001280160.1:n.157+1363C>G
NM_001293233.2:c.316C>G (MYCN)	NP_001280162.1:p.Gln106Glu
NR_161163.1:n.282+46G>C (MYCNOS)