Canonical Allele Identifier: CA2657954348

Gene: MYCN MYCNOS

Linked Data

• gnomAD v4: 2-15942071-AGCTGCTCCACGTCCACCATGCCGGGCATGATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942074_15942106del , CM000664.2:g.15942074_15942106del	GRCh38
NC_000002.11:g.16082196_16082228del , CM000664.1:g.16082196_16082228del	GRCh37
NC_000002.10:g.15999647_15999679del	NCBI36
NG_007457.1:g.6514_6546del

Transcript Alleles

HGVS	Amino-acid change
ENST00000281043.4:c.10_42del (MYCN) MANE Select	ENSP00000281043.3:p.Cys4_Cys14del
ENST00000638417.1:c.157+1331_157+1363del (MYCN)	ENSP00000491476.1:n.157+1331_157+1363del
ENST00000281043.3:c.10_42del (MYCN)	ENSP00000281043.3:p.Cys4_Cys14del
NM_001293228.1:c.10_42del (MYCN)	NP_001280157.1:p.Cys4_Cys14del
NM_001293231.1:c.157+1331_157+1363del (MYCN)	NP_001280160.1:n.157+1331_157+1363del
NM_001293233.1:c.284_316del (MYCN)	NP_001280162.1:p.Leu95_Leu105del
NM_005378.5:c.10_42del (MYCN)	NP_005369.2:p.Cys4_Cys14del
NM_001329968.1:c.-234+48_-234+80del (MYCNOS)	NP_001316897.1:n.-234+48_-234+80del
XM_024452528.1:c.-234+278_-234+310del (MYCNOS)	XP_024308296.1:n.-234+278_-234+310del
NM_005378.6:c.10_42del (MYCN) MANE Select	NP_005369.2:p.Cys4_Cys14del
NM_001293228.2:c.10_42del (MYCN)	NP_001280157.1:p.Cys4_Cys14del
NM_001293231.2:c.157+1331_157+1363del (MYCN)	NP_001280160.1:n.157+1331_157+1363del
NM_001293233.2:c.284_316del (MYCN)	NP_001280162.1:p.Leu95_Leu105del
NR_161163.1:n.282+48_282+80del (MYCNOS)