Canonical Allele Identifier: CA2491131033

Gene: MYCN

Linked Data

• dbSNP Id: rs1662836892
• gnomAD v4: 2-15945484-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945489_15945490del , CM000664.2:g.15945489_15945490del	GRCh38
NC_000002.11:g.16085611_16085612del , CM000664.1:g.16085611_16085612del	GRCh37
NC_000002.10:g.16003062_16003063del	NCBI36
NG_007457.1:g.9929_9930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-4_140-3del
ENST00000281043.4:c.791-4_791-3del MANE Select	ENSP00000281043.3:n.791-4_791-3del
ENST00000638417.1:c.158-4_158-3del	ENSP00000491476.1:n.158-4_158-3del
ENST00000281043.3:c.791-4_791-3del	ENSP00000281043.3:n.791-4_791-3del
NM_001293228.1:c.791-4_791-3del	NP_001280157.1:n.791-4_791-3del
NM_001293231.1:c.158-4_158-3del	NP_001280160.1:n.158-4_158-3del
NM_001293233.1:c.*726-4_*726-3del	NP_001280162.1:n.*726-4_*726-3del
NM_005378.5:c.791-4_791-3del	NP_005369.2:n.791-4_791-3del
NM_005378.6:c.791-4_791-3del MANE Select	NP_005369.2:n.791-4_791-3del
NM_001293228.2:c.791-4_791-3del	NP_001280157.1:n.791-4_791-3del
NM_001293231.2:c.158-4_158-3del	NP_001280160.1:n.158-4_158-3del
NM_001293233.2:c.*726-4_*726-3del	NP_001280162.1:n.*726-4_*726-3del