Canonical Allele Identifier: CA2491131032

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945484_15945486delinsTTC , CM000664.2:g.15945484_15945486delinsTTC	GRCh38
NC_000002.11:g.16085606_16085608delinsTTC , CM000664.1:g.16085606_16085608delinsTTC	GRCh37
NC_000002.10:g.16003057_16003059delinsTTC	NCBI36
NG_007457.1:g.9924_9926delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-9_140-7delinsTTC
ENST00000281043.4:c.791-9_791-7delinsTTC MANE Select	ENSP00000281043.3:n.791-9_791-7delinsTTC
ENST00000638417.1:c.158-9_158-7delinsTTC	ENSP00000491476.1:n.158-9_158-7delinsTTC
ENST00000281043.3:c.791-9_791-7delinsTTC	ENSP00000281043.3:n.791-9_791-7delinsTTC
NM_001293228.1:c.791-9_791-7delinsTTC	NP_001280157.1:n.791-9_791-7delinsTTC
NM_001293231.1:c.158-9_158-7delinsTTC	NP_001280160.1:n.158-9_158-7delinsTTC
NM_001293233.1:c.*726-9_*726-7delinsTTC	NP_001280162.1:n.*726-9_*726-7delinsTTC
NM_005378.5:c.791-9_791-7delinsTTC	NP_005369.2:n.791-9_791-7delinsTTC
NM_005378.6:c.791-9_791-7delinsTTC MANE Select	NP_005369.2:n.791-9_791-7delinsTTC
NM_001293228.2:c.791-9_791-7delinsTTC	NP_001280157.1:n.791-9_791-7delinsTTC
NM_001293231.2:c.158-9_158-7delinsTTC	NP_001280160.1:n.158-9_158-7delinsTTC
NM_001293233.2:c.*726-9_*726-7delinsTTC	NP_001280162.1:n.*726-9_*726-7delinsTTC