Canonical Allele Identifier: CA2657954653

Gene: MYCN

Linked Data

• gnomAD v4: 2-15945624-C-CTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945625_15945627dup , CM000664.2:g.15945625_15945627dup	GRCh38
NC_000002.11:g.16085747_16085749dup , CM000664.1:g.16085747_16085749dup	GRCh37
NC_000002.10:g.16003198_16003200dup	NCBI36
NG_007457.1:g.10065_10067dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.272_274dup
ENST00000281043.4:c.923_925dup MANE Select	ENSP00000281043.3:p.Leu308_Gly309insVal
ENST00000638417.1:c.290_292dup	ENSP00000491476.1:p.Leu97_Gly98insVal
ENST00000281043.3:c.923_925dup	ENSP00000281043.3:p.Leu308_Gly309insVal
NM_001293228.1:c.923_925dup	NP_001280157.1:p.Leu308_Gly309insVal
NM_001293231.1:c.290_292dup	NP_001280160.1:p.Leu97_Gly98insVal
NM_001293233.1:c.*858_*860dup	NP_001280162.1:n.*858_*860dup
NM_005378.5:c.923_925dup	NP_005369.2:p.Leu308_Gly309insVal
NM_005378.6:c.923_925dup MANE Select	NP_005369.2:p.Leu308_Gly309insVal
NM_001293228.2:c.923_925dup	NP_001280157.1:p.Leu308_Gly309insVal
NM_001293231.2:c.290_292dup	NP_001280160.1:p.Leu97_Gly98insVal
NM_001293233.2:c.*858_*860dup	NP_001280162.1:n.*858_*860dup