Canonical Allele Identifier: CA2657954648

Gene: MYCN

Linked Data

• gnomAD v4: 2-15945479-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945480dup , CM000664.2:g.15945480dup	GRCh38
NC_000002.11:g.16085602dup , CM000664.1:g.16085602dup	GRCh37
NC_000002.10:g.16003053dup	NCBI36
NG_007457.1:g.9920dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-13dup
ENST00000281043.4:c.791-13dup MANE Select	ENSP00000281043.3:n.791-13dup
ENST00000638417.1:c.158-13dup	ENSP00000491476.1:n.158-13dup
ENST00000281043.3:c.791-13dup	ENSP00000281043.3:n.791-13dup
NM_001293228.1:c.791-13dup	NP_001280157.1:n.791-13dup
NM_001293231.1:c.158-13dup	NP_001280160.1:n.158-13dup
NM_001293233.1:c.*726-13dup	NP_001280162.1:n.*726-13dup
NM_005378.5:c.791-13dup	NP_005369.2:n.791-13dup
NM_005378.6:c.791-13dup MANE Select	NP_005369.2:n.791-13dup
NM_001293228.2:c.791-13dup	NP_001280157.1:n.791-13dup
NM_001293231.2:c.158-13dup	NP_001280160.1:n.158-13dup
NM_001293233.2:c.*726-13dup	NP_001280162.1:n.*726-13dup