Canonical Allele Identifier: CA2748974664

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945474_15945477del , CM000664.2:g.15945474_15945477del	GRCh38
NC_000002.11:g.16085596_16085599del , CM000664.1:g.16085596_16085599del	GRCh37
NC_000002.10:g.16003047_16003050del	NCBI36
NG_007457.1:g.9914_9917del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-19_140-16del
ENST00000281043.4:c.791-19_791-16del MANE Select	ENSP00000281043.3:n.791-19_791-16del
ENST00000638417.1:c.158-19_158-16del	ENSP00000491476.1:n.158-19_158-16del
ENST00000281043.3:c.791-19_791-16del	ENSP00000281043.3:n.791-19_791-16del
NM_001293228.1:c.791-19_791-16del	NP_001280157.1:n.791-19_791-16del
NM_001293231.1:c.158-19_158-16del	NP_001280160.1:n.158-19_158-16del
NM_001293233.1:c.*726-19_*726-16del	NP_001280162.1:n.*726-19_*726-16del
NM_005378.5:c.791-19_791-16del	NP_005369.2:n.791-19_791-16del
NM_005378.6:c.791-19_791-16del MANE Select	NP_005369.2:n.791-19_791-16del
NM_001293228.2:c.791-19_791-16del	NP_001280157.1:n.791-19_791-16del
NM_001293231.2:c.158-19_158-16del	NP_001280160.1:n.158-19_158-16del
NM_001293233.2:c.*726-19_*726-16del	NP_001280162.1:n.*726-19_*726-16del