Canonical Allele Identifier: CA916317349
Gene: LMNA HGNC NCBI

Linked Data

dbSNP Id: rs1558134813

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156138487_156138495dup , CM000663.2:g.156138487_156138495dup GRCh38
NC_000001.10:g.156108278_156108286dup , CM000663.1:g.156108278_156108286dup GRCh37
NC_000001.9:g.154374902_154374910dup NCBI36
NG_008692.2:g.60915_60923dup , LRG_254:g.60915_60923dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.1141-1_1148dup
ENST00000682650.1:c.1609-1_1616dup
ENST00000683032.1:c.1699-1_1706dup
ENST00000683773.1:n.44-1_51dup
ENST00000684195.1:c.*790_*798dup ENSP00000508220.1:n.*790_*798dup
ENST00000361308.9:c.1699-1_1706dup
ENST00000368300.9:c.1699-1_1706dup
ENST00000496738.6:n.2901_2909dup
ENST00000674518.1:c.*1049-1_*1056dup
ENST00000674600.1:c.*1498-1_*1505dup
ENST00000674720.1:c.*1004_*1012dup ENSP00000502798.1:n.*1004_*1012dup
ENST00000675455.1:c.*1499-1_*1506dup
ENST00000675667.1:c.1699-1_1706dup
ENST00000675874.1:c.*1170-1_*1177dup
ENST00000675881.1:c.*710-1_*717dup
ENST00000675939.1:c.1699-1_1706dup
ENST00000675989.1:n.3301_3309dup
ENST00000676208.1:c.*802-1_*809dup
ENST00000676283.1:n.3238_3246dup
ENST00000676385.2:c.1609-1_1616dup
ENST00000676434.1:c.*1453_*1461dup ENSP00000501648.1:n.*1453_*1461dup
ENST00000347559.6:c.1609-1_1616dup
ENST00000368299.7:c.1699-1_1706dup
ENST00000368300.8:c.1699-1_1706dup
ENST00000448611.6:c.1363-1_1370dup
ENST00000473598.6:c.1402-1_1409dup
ENST00000496738.5:n.1911_1919dup
ENST00000506981.1:n.283-1_290dup
ENST00000508500.1:c.487-1_494dup
NM_001257374.2:c.1363-1_1370dup
NM_001282626.1:c.1699-1_1706dup
NM_170707.3:c.1699-1_1706dup
NM_170708.3:c.1609-1_1616dup
XM_011509533.1:c.1363-1_1370dup
XM_011509534.1:c.1075-1_1082dup
XR_921781.1:n.1988-1_1995dup
XM_011509534.2:c.1075-1_1082dup
XR_921781.2:n.1986-1_1993dup
NM_170707.4:c.1699-1_1706dup
NM_001257374.3:c.1363-1_1370dup
NM_001282626.2:c.1699-1_1706dup
NM_170708.4:c.1609-1_1616dup