Canonical Allele Identifier: CA2576682125

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945577_15945588del , CM000664.2:g.15945577_15945588del	GRCh38
NC_000002.11:g.16085699_16085710del , CM000664.1:g.16085699_16085710del	GRCh37
NC_000002.10:g.16003150_16003161del	NCBI36
NG_007457.1:g.10017_10028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.224_235del
ENST00000281043.4:c.875_886del MANE Select	ENSP00000281043.3:p.Lys292_Thr295del
ENST00000638417.1:c.242_253del	ENSP00000491476.1:p.Lys81_Thr84del
ENST00000281043.3:c.875_886del	ENSP00000281043.3:p.Lys292_Thr295del
NM_001293228.1:c.875_886del	NP_001280157.1:p.Lys292_Thr295del
NM_001293231.1:c.242_253del	NP_001280160.1:p.Lys81_Thr84del
NM_001293233.1:c.*810_*821del	NP_001280162.1:n.*810_*821del
NM_005378.5:c.875_886del	NP_005369.2:p.Lys292_Thr295del
NM_005378.6:c.875_886del MANE Select	NP_005369.2:p.Lys292_Thr295del
NM_001293228.2:c.875_886del	NP_001280157.1:p.Lys292_Thr295del
NM_001293231.2:c.242_253del	NP_001280160.1:p.Lys81_Thr84del
NM_001293233.2:c.*810_*821del	NP_001280162.1:n.*810_*821del