Canonical Allele Identifier: CA2576682123

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945453_15945454del , CM000664.2:g.15945453_15945454del	GRCh38
NC_000002.11:g.16085575_16085576del , CM000664.1:g.16085575_16085576del	GRCh37
NC_000002.10:g.16003026_16003027del	NCBI36
NG_007457.1:g.9893_9894del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-40_140-39del
ENST00000281043.4:c.791-40_791-39del MANE Select	ENSP00000281043.3:n.791-40_791-39del
ENST00000638417.1:c.158-40_158-39del	ENSP00000491476.1:n.158-40_158-39del
ENST00000281043.3:c.791-40_791-39del	ENSP00000281043.3:n.791-40_791-39del
NM_001293228.1:c.791-40_791-39del	NP_001280157.1:n.791-40_791-39del
NM_001293231.1:c.158-40_158-39del	NP_001280160.1:n.158-40_158-39del
NM_001293233.1:c.*726-40_*726-39del	NP_001280162.1:n.*726-40_*726-39del
NM_005378.5:c.791-40_791-39del	NP_005369.2:n.791-40_791-39del
NM_005378.6:c.791-40_791-39del MANE Select	NP_005369.2:n.791-40_791-39del
NM_001293228.2:c.791-40_791-39del	NP_001280157.1:n.791-40_791-39del
NM_001293231.2:c.158-40_158-39del	NP_001280160.1:n.158-40_158-39del
NM_001293233.2:c.*726-40_*726-39del	NP_001280162.1:n.*726-40_*726-39del