Canonical Allele Identifier: CA345930008

Gene: MYCN MYCNOS

Linked Data

• MyVariant Identifiers: chr2:g.16082223A>G (hg19) ; chr2:g.15942101A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942101A>G , CM000664.2:g.15942101A>G	GRCh38
NC_000002.11:g.16082223A>G , CM000664.1:g.16082223A>G	GRCh37
NC_000002.10:g.15999674A>G	NCBI36
NG_007457.1:g.6541A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281043.4:c.37A>G (MYCN) MANE Select	ENSP00000281043.3:p.Ile13Val
ENST00000638417.1:c.157+1358A>G (MYCN)	ENSP00000491476.1:n.157+1358A>G
ENST00000281043.3:c.37A>G (MYCN)	ENSP00000281043.3:p.Ile13Val
NM_001293228.1:c.37A>G (MYCN)	NP_001280157.1:p.Ile13Val
NM_001293231.1:c.157+1358A>G (MYCN)	NP_001280160.1:n.157+1358A>G
NM_001293233.1:c.311A>G (MYCN)	NP_001280162.1:p.Asp104Gly
NM_005378.5:c.37A>G (MYCN)	NP_005369.2:p.Ile13Val
NM_001329968.1:c.-234+51T>C (MYCNOS)	NP_001316897.1:n.-234+51T>C
XM_024452528.1:c.-234+281T>C (MYCNOS)	XP_024308296.1:n.-234+281T>C
NM_005378.6:c.37A>G (MYCN) MANE Select	NP_005369.2:p.Ile13Val
NM_001293228.2:c.37A>G (MYCN)	NP_001280157.1:p.Ile13Val
NM_001293231.2:c.157+1358A>G (MYCN)	NP_001280160.1:n.157+1358A>G
NM_001293233.2:c.311A>G (MYCN)	NP_001280162.1:p.Asp104Gly
NR_161163.1:n.282+51T>C (MYCNOS)