Canonical Allele Identifier: CA1200473475
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156138503A= , CM000663.2:g.156138503A= GRCh38
NC_000001.10:g.156108294A= , CM000663.1:g.156108294A= GRCh37
NC_000001.9:g.154374918A= NCBI36
NG_008692.2:g.60931A= , LRG_254:g.60931A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1156A= ENSP00000426535.3:p.Ser386=
ENST00000682650.1:c.1624A= ENSP00000506904.1:p.Ser542=
ENST00000683032.1:c.1714A= ENSP00000506771.1:p.Ser572=
ENST00000683773.1:n.59A=
ENST00000684195.1:c.*806A= ENSP00000508220.1:n.*806A=
ENST00000361308.9:c.1714A= ENSP00000355292.6:p.Ser572=
ENST00000368300.9:c.1714A= MANE Select ENSP00000357283.4:p.Ser572=
ENST00000496738.6:n.2917A=
ENST00000674518.1:c.*1064A= ENSP00000502261.1:n.*1064A=
ENST00000674600.1:c.*1513A= ENSP00000501666.1:n.*1513A=
ENST00000674720.1:c.*1020A= ENSP00000502798.1:n.*1020A=
ENST00000675455.1:c.*1514A= ENSP00000501795.1:n.*1514A=
ENST00000675667.1:c.1714A= ENSP00000501803.1:p.Ser572=
ENST00000675874.1:c.*1185A= ENSP00000501851.1:n.*1185A=
ENST00000675881.1:c.*725A= ENSP00000501670.1:n.*725A=
ENST00000675939.1:c.1714A= ENSP00000502256.1:p.Ser572=
ENST00000675989.1:n.3317A=
ENST00000676208.1:c.*817A= ENSP00000502468.1:n.*817A=
ENST00000676283.1:n.3254A=
ENST00000676385.2:c.1624A= ENSP00000502091.1:p.Ser542=
ENST00000676434.1:c.*1469A= ENSP00000501648.1:n.*1469A=
ENST00000347559.6:c.1624A= ENSP00000292304.3:p.Ser542=
ENST00000368299.7:c.1714A= ENSP00000357282.3:p.Ser572=
ENST00000368300.8:c.1714A= ENSP00000357283.4:p.Ser572=
ENST00000448611.6:c.1378A= ENSP00000395597.2:p.Ser460=
ENST00000473598.6:c.1417A= ENSP00000421821.1:p.Ser473=
ENST00000496738.5:n.1927A=
ENST00000506981.1:n.298A=
ENST00000508500.1:c.502A= ENSP00000424977.1:p.Ser168=
NM_001257374.2:c.1378A= NP_001244303.1:p.Ser460=
NM_001282626.1:c.1714A= NP_001269555.1:p.Ser572=
NM_170707.3:c.1714A= NP_733821.1:p.Ser572=
NM_170708.3:c.1624A= NP_733822.1:p.Ser542=
XM_011509533.1:c.1378A= XP_011507835.1:p.Ser460=
XM_011509534.1:c.1090A= XP_011507836.1:p.Ser364=
XR_921781.1:n.2003A=
XM_011509534.2:c.1090A= XP_011507836.1:p.Ser364=
XR_921781.2:n.2001A=
NM_170707.4:c.1714A= MANE Select NP_733821.1:p.Ser572=
NM_001257374.3:c.1378A= NP_001244303.1:p.Ser460=
NM_001282626.2:c.1714A= NP_001269555.1:p.Ser572=
NM_170708.4:c.1624A= NP_733822.1:p.Ser542=