Canonical Allele Identifier: CA345931601

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085613A>C (hg19) ; chr2:g.15945491A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945491A>C , CM000664.2:g.15945491A>C	GRCh38
NC_000002.11:g.16085613A>C , CM000664.1:g.16085613A>C	GRCh37
NC_000002.10:g.16003064A>C	NCBI36
NG_007457.1:g.9931A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-2A>C
ENST00000281043.4:c.791-2A>C MANE Select	ENSP00000281043.3:n.791-2A>C
ENST00000638417.1:c.158-2A>C	ENSP00000491476.1:n.158-2A>C
ENST00000281043.3:c.791-2A>C	ENSP00000281043.3:n.791-2A>C
NM_001293228.1:c.791-2A>C	NP_001280157.1:n.791-2A>C
NM_001293231.1:c.158-2A>C	NP_001280160.1:n.158-2A>C
NM_001293233.1:c.*726-2A>C	NP_001280162.1:n.*726-2A>C
NM_005378.5:c.791-2A>C	NP_005369.2:n.791-2A>C
NM_005378.6:c.791-2A>C MANE Select	NP_005369.2:n.791-2A>C
NM_001293228.2:c.791-2A>C	NP_001280157.1:n.791-2A>C
NM_001293231.2:c.158-2A>C	NP_001280160.1:n.158-2A>C
NM_001293233.2:c.*726-2A>C	NP_001280162.1:n.*726-2A>C