Canonical Allele Identifier: CA413414466
Gene: MSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.65716855A>C , CM000685.2:g.65716855A>C GRCh38
NC_000023.10:g.64936717A>C , CM000685.1:g.64936717A>C GRCh37
NC_000023.9:g.64853442A>C NCBI36
NG_012516.1:g.54207A>C

Transcript Alleles

HGVS Amino-acid Change
NM_002444.3:c.50A>C MANE Select NP_002435.1:p.Glu17Ala
ENST00000360270.7:c.50A>C MANE Select ENSP00000353408.5:p.Glu17Ala
NM_002444.2:c.50A>C NP_002435.1:p.Glu17Ala
ENST00000360270.6:c.50A>C ENSP00000353408.5:p.Glu17Ala
ENST00000609672.5:c.17A>C ENSP00000477441.1:p.Glu6Ala
ENST00000697133.1:c.17A>C ENSP00000513131.1:p.Glu6Ala
ENST00000697134.1:c.*22A>C ENSP00000513132.1:n.*22A>C
ENST00000697135.1:n.238A>C
ENST00000697136.1:n.183A>C
ENST00000697137.1:c.17A>C ENSP00000513133.1:p.Glu6Ala
ENST00000697138.1:c.17A>C ENSP00000513134.1:p.Glu6Ala
ENST00000697139.1:n.155A>C
ENST00000697140.1:n.164A>C
XM_005262269.2:c.53A>C XP_005262326.1:p.Glu18Ala
XM_011530959.1:c.149A>C XP_011529261.1:p.Glu50Ala
XM_011530960.1:c.17A>C XP_011529262.1:p.Glu6Ala
XM_017029545.1:c.17A>C XP_016885034.1:p.Glu6Ala
XM_017029546.1:c.17A>C XP_016885035.1:p.Glu6Ala