Canonical Allele Identifier: CA2657954664
Gene: MYCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945886_15945909dup , CM000664.2:g.15945886_15945909dup GRCh38
NC_000002.11:g.16086008_16086031dup , CM000664.1:g.16086008_16086031dup GRCh37
NC_000002.10:g.16003459_16003482dup NCBI36
NG_007457.1:g.10326_10349dup

Transcript Alleles

HGVS Amino-acid change
ENST00000703162.1:n.533_556dup
ENST00000281043.4:c.1184_1207dup MANE Select ENSP00000281043.3:p.Leu402_Thr403insAsnAs...
ENST00000638417.1:c.551_574dup ENSP00000491476.1:p.Leu191_Thr192insAsnAs...
ENST00000281043.3:c.1184_1207dup ENSP00000281043.3:p.Leu402_Thr403insAsnAs...
NM_001293228.1:c.1184_1207dup NP_001280157.1:p.Leu402_Thr403insAsnAspLe...
NM_001293231.1:c.551_574dup NP_001280160.1:p.Leu191_Thr192insAsnAspLe...
NM_001293233.1:c.*1119_*1142dup NP_001280162.1:n.*1119_*1142dup
NM_005378.5:c.1184_1207dup NP_005369.2:p.Leu402_Thr403insAsnAspLeuAr...
NM_005378.6:c.1184_1207dup MANE Select NP_005369.2:p.Leu402_Thr403insAsnAspLeuAr...
NM_001293228.2:c.1184_1207dup NP_001280157.1:p.Leu402_Thr403insAsnAspLe...
NM_001293231.2:c.551_574dup NP_001280160.1:p.Leu191_Thr192insAsnAspLe...
NM_001293233.2:c.*1119_*1142dup NP_001280162.1:n.*1119_*1142dup