Canonical Allele Identifier: CA1140708220
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156134838C= , CM000663.2:g.156134838C= GRCh38
NC_000001.10:g.156104629C= , CM000663.1:g.156104629C= GRCh37
NC_000001.9:g.154371253C= NCBI36
NG_008692.2:g.57266C= , LRG_254:g.57266C=

Transcript Alleles

HGVS Amino-acid change
ENST00000504687.7:c.115C= ENSP00000426535.3:p.Arg39=
ENST00000682650.1:c.673C= ENSP00000506904.1:p.Arg225=
ENST00000683032.1:c.673C= ENSP00000506771.1:p.Arg225=
ENST00000684195.1:c.673C= ENSP00000508220.1:p.Arg225=
ENST00000361308.9:c.673C= ENSP00000355292.6:p.Arg225=
ENST00000368300.9:c.673C= MANE Select ENSP00000357283.4:p.Arg225=
ENST00000496738.6:n.1048C=
ENST00000504687.6:c.9C= ENSP00000426535.2:p.Pro3=
ENST00000674518.1:c.*23C= ENSP00000502261.1:n.*23C=
ENST00000674600.1:c.*472C= ENSP00000501666.1:n.*472C=
ENST00000674720.1:c.673C= ENSP00000502798.1:p.Arg225=
ENST00000675431.1:n.366C=
ENST00000675455.1:c.*473C= ENSP00000501795.1:n.*473C=
ENST00000675667.1:c.673C= ENSP00000501803.1:p.Arg225=
ENST00000675874.1:c.*144C= ENSP00000501851.1:n.*144C=
ENST00000675881.1:c.673C= ENSP00000501670.1:p.Arg225=
ENST00000675939.1:c.673C= ENSP00000502256.1:p.Arg225=
ENST00000675989.1:n.1048C=
ENST00000676208.1:c.673C= ENSP00000502468.1:p.Arg225=
ENST00000676283.1:n.1048C=
ENST00000676385.2:c.673C= ENSP00000502091.1:p.Arg225=
ENST00000676434.1:c.673C= ENSP00000501648.1:p.Arg225=
ENST00000677389.1:c.673C= MANE Plus Clinical ENSP00000503633.1:p.Arg225=
ENST00000347559.6:c.673C= ENSP00000292304.3:p.Arg225=
ENST00000361308.8:c.673C= ENSP00000355292.5:p.Arg225=
ENST00000368297.5:c.430C= ENSP00000357280.1:p.Arg144=
ENST00000368299.7:c.673C= ENSP00000357282.3:p.Arg225=
ENST00000368300.8:c.673C= ENSP00000357283.4:p.Arg225=
ENST00000368301.6:c.673C= ENSP00000357284.2:p.Arg225=
ENST00000448611.6:c.337C= ENSP00000395597.2:p.Arg113=
ENST00000473598.6:c.376C= ENSP00000421821.1:p.Arg126=
ENST00000496738.5:n.18C=
ENST00000504687.5:c.424C= ENSP00000426535.1:p.Arg142=
ENST00000515459.5:c.*347C= ENSP00000424518.1:n.*347C=
ENST00000515824.1:n.34C=
NM_001257374.2:c.337C= NP_001244303.1:p.Arg113=
NM_001282624.1:c.430C= NP_001269553.1:p.Arg144=
NM_001282625.1:c.673C= NP_001269554.1:p.Arg225=
NM_001282626.1:c.673C= NP_001269555.1:p.Arg225=
NM_005572.3:c.673C= , LRG_254t1:c.673C= NP_005563.1:p.Arg225=
NM_170707.3:c.673C= NP_733821.1:p.Arg225=
NM_170708.3:c.673C= NP_733822.1:p.Arg225=
XM_011509533.1:c.337C= XP_011507835.1:p.Arg113=
XM_011509534.1:c.9C= XP_011507836.1:p.Pro3=
XR_921781.1:n.922C=
XM_011509534.2:c.9C= XP_011507836.1:p.Pro3=
XR_921781.2:n.920C=
NM_170707.4:c.673C= MANE Select NP_733821.1:p.Arg225=
NM_001257374.3:c.337C= NP_001244303.1:p.Arg113=
NM_001282626.2:c.673C= NP_001269555.1:p.Arg225=
NM_001282624.2:c.430C= NP_001269553.1:p.Arg144=
NM_001282625.2:c.673C= NP_001269554.1:p.Arg225=
NM_005572.4:c.673C= MANE Plus Clinical NP_005563.1:p.Arg225=
NM_170708.4:c.673C= NP_733822.1:p.Arg225=