Canonical Allele Identifier: CA413412693
Community Standard Title: NM_002444.3(MSN):c.874A>C (p.Met292Leu)
Gene: MSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.65735345A>C , CM000685.2:g.65735345A>C GRCh38
NC_000023.10:g.64955207A>C , CM000685.1:g.64955207A>C GRCh37
NC_000023.9:g.64871932A>C NCBI36
NG_012516.1:g.72697A>C

Transcript Alleles

HGVS Amino-acid Change
NM_002444.3:c.874A>C MANE Select NP_002435.1:p.Met292Leu
ENST00000360270.7:c.874A>C MANE Select ENSP00000353408.5:p.Met292Leu
NM_002444.2:c.874A>C NP_002435.1:p.Met292Leu
ENST00000360270.6:c.874A>C ENSP00000353408.5:p.Met292Leu
ENST00000697133.1:c.841A>C ENSP00000513131.1:p.Met281Leu
ENST00000697134.1:c.*846A>C ENSP00000513132.1:n.*846A>C
ENST00000697135.1:n.2456A>C
ENST00000697137.1:c.841A>C ENSP00000513133.1:p.Met281Leu
ENST00000697138.1:c.841A>C ENSP00000513134.1:p.Met281Leu
ENST00000697140.1:n.988A>C
XM_005262269.2:c.877A>C XP_005262326.1:p.Met293Leu
XM_011530959.1:c.973A>C XP_011529261.1:p.Met325Leu
XM_011530960.1:c.841A>C XP_011529262.1:p.Met281Leu
XM_017029545.1:c.841A>C XP_016885034.1:p.Met281Leu
XM_017029546.1:c.841A>C XP_016885035.1:p.Met281Leu