Canonical Allele Identifier: CA2573055377
Gene: MSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.65736891del , CM000685.2:g.65736891del GRCh38
NC_000023.10:g.64956753del , CM000685.1:g.64956753del GRCh37
NC_000023.9:g.64873478del NCBI36
NG_012516.1:g.74243del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697133.1:c.1023del ENSP00000513131.1:p.Lys341AsnfsTer?
ENST00000697134.1:c.*1028del ENSP00000513132.1:n.*1028del
ENST00000697135.1:n.2638del
ENST00000697137.1:c.1023del ENSP00000513133.1:p.Lys341AsnfsTer?
ENST00000697138.1:c.1023del ENSP00000513134.1:p.Lys341AsnfsTer?
ENST00000697140.1:n.1170del
ENST00000697142.1:n.973del
ENST00000360270.7:c.1056del MANE Select ENSP00000353408.5:p.Lys352AsnfsTer?
ENST00000360270.6:c.1056del ENSP00000353408.5:p.Lys352AsnfsTer?
NM_002444.2:c.1056del NP_002435.1:p.Lys352AsnfsTer?
XM_005262269.2:c.1059del XP_005262326.1:p.Lys353AsnfsTer?
XM_011530959.1:c.1155del XP_011529261.1:p.Lys385AsnfsTer?
XM_011530960.1:c.1023del XP_011529262.1:p.Lys341AsnfsTer?
XM_017029545.1:c.1023del XP_016885034.1:p.Lys341AsnfsTer?
XM_017029546.1:c.1023del XP_016885035.1:p.Lys341AsnfsTer?
NM_002444.3:c.1056del MANE Select NP_002435.1:p.Lys352AsnfsTer?