Canonical Allele Identifier: CA2580063664

Gene: MYCN MYCNOS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942392del , CM000664.2:g.15942392del	GRCh38
NC_000002.11:g.16082514del , CM000664.1:g.16082514del	GRCh37
NC_000002.10:g.15999965del	NCBI36
NG_007457.1:g.6832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281043.4:c.328del (MYCN) MANE Select	ENSP00000281043.3:p.Val110SerfsTer21
ENST00000638417.1:c.157+1649del (MYCN)	ENSP00000491476.1:n.157+1649del
ENST00000281043.3:c.328del (MYCN)	ENSP00000281043.3:p.Val110SerfsTer21
NM_001293228.1:c.328del (MYCN)	NP_001280157.1:p.Val110SerfsTer21
NM_001293231.1:c.157+1649del (MYCN)	NP_001280160.1:n.157+1649del
NM_001293233.1:c.*263del (MYCN)	NP_001280162.1:n.*263del
NM_005378.5:c.328del (MYCN)	NP_005369.2:p.Val110SerfsTer21
XM_024452528.1:c.-243del (MYCNOS)	XP_024308296.1:n.-243del
NM_005378.6:c.328del (MYCN) MANE Select	NP_005369.2:p.Val110SerfsTer21
NM_001293228.2:c.328del (MYCN)	NP_001280157.1:p.Val110SerfsTer21
NM_001293231.2:c.157+1649del (MYCN)	NP_001280160.1:n.157+1649del
NM_001293233.2:c.*263del (MYCN)	NP_001280162.1:n.*263del
NR_161163.1:n.43del (MYCNOS)