Canonical Allele Identifier: CA345931958

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085780T>C (hg19) ; chr2:g.15945658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945658T>C , CM000664.2:g.15945658T>C	GRCh38
NC_000002.11:g.16085780T>C , CM000664.1:g.16085780T>C	GRCh37
NC_000002.10:g.16003231T>C	NCBI36
NG_007457.1:g.10098T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.305T>C
ENST00000281043.4:c.956T>C MANE Select	ENSP00000281043.3:p.Ile319Thr
ENST00000638417.1:c.323T>C	ENSP00000491476.1:p.Ile108Thr
ENST00000281043.3:c.956T>C	ENSP00000281043.3:p.Ile319Thr
NM_001293228.1:c.956T>C	NP_001280157.1:p.Ile319Thr
NM_001293231.1:c.323T>C	NP_001280160.1:p.Ile108Thr
NM_001293233.1:c.*891T>C	NP_001280162.1:n.*891T>C
NM_005378.5:c.956T>C	NP_005369.2:p.Ile319Thr
NM_005378.6:c.956T>C MANE Select	NP_005369.2:p.Ile319Thr
NM_001293228.2:c.956T>C	NP_001280157.1:p.Ile319Thr
NM_001293231.2:c.323T>C	NP_001280160.1:p.Ile108Thr
NM_001293233.2:c.*891T>C	NP_001280162.1:n.*891T>C