Canonical Allele Identifier: CA2657954661

Gene: MYCN

Linked Data

• gnomAD v4: 2-15945870-GAGCGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945877_15945882del , CM000664.2:g.15945877_15945882del	GRCh38
NC_000002.11:g.16085999_16086004del , CM000664.1:g.16085999_16086004del	GRCh37
NC_000002.10:g.16003450_16003455del	NCBI36
NG_007457.1:g.10317_10322del

Transcript Alleles

HGVS	Amino-acid change
ENST00000703162.1:n.524_529del
ENST00000281043.4:c.1175_1180del MANE Select	ENSP00000281043.3:p.Gln392_Arg393del
ENST00000638417.1:c.542_547del	ENSP00000491476.1:p.Gln181_Arg182del
ENST00000281043.3:c.1175_1180del	ENSP00000281043.3:p.Gln392_Arg393del
NM_001293228.1:c.1175_1180del	NP_001280157.1:p.Gln392_Arg393del
NM_001293231.1:c.542_547del	NP_001280160.1:p.Gln181_Arg182del
NM_001293233.1:c.*1110_*1115del	NP_001280162.1:n.*1110_*1115del
NM_005378.5:c.1175_1180del	NP_005369.2:p.Gln392_Arg393del
NM_005378.6:c.1175_1180del MANE Select	NP_005369.2:p.Gln392_Arg393del
NM_001293228.2:c.1175_1180del	NP_001280157.1:p.Gln392_Arg393del
NM_001293231.2:c.542_547del	NP_001280160.1:p.Gln181_Arg182del
NM_001293233.2:c.*1110_*1115del	NP_001280162.1:n.*1110_*1115del