Canonical Allele Identifier: CA2491131025

Gene: MYCN

Linked Data

• dbSNP Id: rs1662836560

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945468_15945471del , CM000664.2:g.15945468_15945471del	GRCh38
NC_000002.11:g.16085590_16085593del , CM000664.1:g.16085590_16085593del	GRCh37
NC_000002.10:g.16003041_16003044del	NCBI36
NG_007457.1:g.9908_9911del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-25_140-22del
ENST00000281043.4:c.791-25_791-22del MANE Select	ENSP00000281043.3:n.791-25_791-22del
ENST00000638417.1:c.158-25_158-22del	ENSP00000491476.1:n.158-25_158-22del
ENST00000281043.3:c.791-25_791-22del	ENSP00000281043.3:n.791-25_791-22del
NM_001293228.1:c.791-25_791-22del	NP_001280157.1:n.791-25_791-22del
NM_001293231.1:c.158-25_158-22del	NP_001280160.1:n.158-25_158-22del
NM_001293233.1:c.*726-25_*726-22del	NP_001280162.1:n.*726-25_*726-22del
NM_005378.5:c.791-25_791-22del	NP_005369.2:n.791-25_791-22del
NM_005378.6:c.791-25_791-22del MANE Select	NP_005369.2:n.791-25_791-22del
NM_001293228.2:c.791-25_791-22del	NP_001280157.1:n.791-25_791-22del
NM_001293231.2:c.158-25_158-22del	NP_001280160.1:n.158-25_158-22del
NM_001293233.2:c.*726-25_*726-22del	NP_001280162.1:n.*726-25_*726-22del