Canonical Allele Identifier: CA413413162

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65736899A>G , CM000685.2:g.65736899A>G	GRCh38
NC_000023.10:g.64956761A>G , CM000685.1:g.64956761A>G	GRCh37
NC_000023.9:g.64873486A>G	NCBI36
NG_012516.1:g.74251A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697133.1:c.1031A>G	ENSP00000513131.1:p.Glu344Gly
ENST00000697134.1:c.*1036A>G	ENSP00000513132.1:n.*1036A>G
ENST00000697135.1:n.2646A>G
ENST00000697137.1:c.1031A>G	ENSP00000513133.1:p.Glu344Gly
ENST00000697138.1:c.1031A>G	ENSP00000513134.1:p.Glu344Gly
ENST00000697140.1:n.1178A>G
ENST00000697142.1:n.981A>G
ENST00000360270.7:c.1064A>G MANE Select	ENSP00000353408.5:p.Glu355Gly
ENST00000360270.6:c.1064A>G	ENSP00000353408.5:p.Glu355Gly
NM_002444.2:c.1064A>G	NP_002435.1:p.Glu355Gly
XM_005262269.2:c.1067A>G	XP_005262326.1:p.Glu356Gly
XM_011530959.1:c.1163A>G	XP_011529261.1:p.Glu388Gly
XM_011530960.1:c.1031A>G	XP_011529262.1:p.Glu344Gly
XM_017029545.1:c.1031A>G	XP_016885034.1:p.Glu344Gly
XM_017029546.1:c.1031A>G	XP_016885035.1:p.Glu344Gly
NM_002444.3:c.1064A>G MANE Select	NP_002435.1:p.Glu355Gly