Canonical Allele Identifier: CA531217869

Gene: MYCN

Linked Data

• dbSNP Id: rs1380519123
• gnomAD v2: 2-16085576-AT-A
• gnomAD v4: 2-15945454-AT-A
• MyVariant Identifiers: chr2:g.16085577del (hg19) ; chr2:g.15945455del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945455del , CM000664.2:g.15945455del	GRCh38
NC_000002.11:g.16085577del , CM000664.1:g.16085577del	GRCh37
NC_000002.10:g.16003028del	NCBI36
NG_007457.1:g.9895del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-38del
ENST00000281043.4:c.791-38del MANE Select	ENSP00000281043.3:n.791-38del
ENST00000638417.1:c.158-38del	ENSP00000491476.1:n.158-38del
ENST00000281043.3:c.791-38del	ENSP00000281043.3:n.791-38del
NM_001293228.1:c.791-38del	NP_001280157.1:n.791-38del
NM_001293231.1:c.158-38del	NP_001280160.1:n.158-38del
NM_001293233.1:c.*726-38del	NP_001280162.1:n.*726-38del
NM_005378.5:c.791-38del	NP_005369.2:n.791-38del
NM_005378.6:c.791-38del MANE Select	NP_005369.2:n.791-38del
NM_001293228.2:c.791-38del	NP_001280157.1:n.791-38del
NM_001293231.2:c.158-38del	NP_001280160.1:n.158-38del
NM_001293233.2:c.*726-38del	NP_001280162.1:n.*726-38del