Canonical Allele Identifier: CA10588313

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945826_15945827del , CM000664.2:g.15945826_15945827del	GRCh38
NC_000002.11:g.16085948_16085949del , CM000664.1:g.16085948_16085949del	GRCh37
NC_000002.10:g.16003399_16003400del	NCBI36
NG_007457.1:g.10266_10267del

Transcript Alleles

HGVS	Amino-acid Change
NM_005378.6:c.1124_1125del MANE Select	NP_005369.2:p.Ser375Ter
ENST00000281043.4:c.1124_1125del MANE Select	ENSP00000281043.3:p.Ser375Ter
NM_001293228.1:c.1124_1125del	NP_001280157.1:p.Ser375Ter
NM_001293228.2:c.1124_1125del	NP_001280157.1:p.Ser375Ter
NM_001293231.1:c.491_492del	NP_001280160.1:p.Ser164Ter
NM_001293231.2:c.491_492del	NP_001280160.1:p.Ser164Ter
NM_001293233.1:c.*1059_*1060del	NP_001280162.1:n.*1059_*1060del
NM_001293233.2:c.*1059_*1060del	NP_001280162.1:n.*1059_*1060del
NM_005378.5:c.1124_1125del	NP_005369.2:p.Ser375Ter
ENST00000281043.3:c.1124_1125del	ENSP00000281043.3:p.Ser375Ter
ENST00000638417.1:c.491_492del	ENSP00000491476.1:p.Ser164Ter
ENST00000703162.1:n.473_474del