Canonical Allele Identifier: CA1200473654
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156138892C= , CM000663.2:g.156138892C= GRCh38
NC_000001.10:g.156108683C= , CM000663.1:g.156108683C= GRCh37
NC_000001.9:g.154375307C= NCBI36
NG_008692.2:g.61320C= , LRG_254:g.61320C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1410+135C= ENSP00000426535.3:n.1410+135C=
ENST00000682650.1:c.1878+135C= ENSP00000506904.1:n.1878+135C=
ENST00000683032.1:c.1968+135C= ENSP00000506771.1:n.1968+135C=
ENST00000683773.1:n.163+285C=
ENST00000684195.1:c.*1060+135C= ENSP00000508220.1:n.*1060+135C=
ENST00000361308.9:c.1968+135C= ENSP00000355292.6:n.1968+135C=
ENST00000368300.9:c.1968+135C= MANE Select ENSP00000357283.4:n.1968+135C=
ENST00000674518.1:c.*1318+135C= ENSP00000502261.1:n.*1318+135C=
ENST00000674600.1:c.*1767+135C= ENSP00000501666.1:n.*1767+135C=
ENST00000675455.1:c.*1768+135C= ENSP00000501795.1:n.*1768+135C=
ENST00000675667.1:c.2103C= ENSP00000501803.1:p.His701=
ENST00000675874.1:c.*1439+135C= ENSP00000501851.1:n.*1439+135C=
ENST00000675881.1:c.*979+135C= ENSP00000501670.1:n.*979+135C=
ENST00000675939.1:c.1968+135C= ENSP00000502256.1:n.1968+135C=
ENST00000675989.1:n.3571+135C=
ENST00000676208.1:c.*1071+135C= ENSP00000502468.1:n.*1071+135C=
ENST00000676385.2:c.1878+135C= ENSP00000502091.1:n.1878+135C=
ENST00000676434.1:c.*1858C= ENSP00000501648.1:n.*1858C=
ENST00000347559.6:c.1878+135C= ENSP00000292304.3:n.1878+135C=
ENST00000368299.7:c.1819-188C= ENSP00000357282.3:n.1819-188C=
ENST00000368300.8:c.1968+135C= ENSP00000357283.4:n.1968+135C=
ENST00000448611.6:c.1632+135C= ENSP00000395597.2:n.1632+135C=
ENST00000473598.6:c.1671+135C= ENSP00000421821.1:n.1671+135C=
ENST00000496738.5:n.2181+135C=
ENST00000506981.1:n.552+135C=
ENST00000508500.1:c.756+135C= ENSP00000424977.1:n.756+135C=
NM_001257374.2:c.1632+135C= NP_001244303.1:n.1632+135C=
NM_001282626.1:c.1819-188C= NP_001269555.1:n.1819-188C=
NM_170707.3:c.1968+135C= NP_733821.1:n.1968+135C=
NM_170708.3:c.1878+135C= NP_733822.1:n.1878+135C=
XM_011509533.1:c.1632+135C= XP_011507835.1:n.1632+135C=
XM_011509534.1:c.1344+135C= XP_011507836.1:n.1344+135C=
XR_921781.1:n.2257+135C=
XM_011509534.2:c.1344+135C= XP_011507836.1:n.1344+135C=
XR_921781.2:n.2255+135C=
NM_170707.4:c.1968+135C= MANE Select NP_733821.1:n.1968+135C=
NM_001257374.3:c.1632+135C= NP_001244303.1:n.1632+135C=
NM_001282626.2:c.1819-188C= NP_001269555.1:n.1819-188C=
NM_170708.4:c.1878+135C= NP_733822.1:n.1878+135C=