Canonical Allele Identifier: CA421068822
Gene: LMNA HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.156106717G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136926G>A , CM000663.2:g.156136926G>A GRCh38
NC_000001.10:g.156106717G>A , CM000663.1:g.156106717G>A GRCh37
NC_000001.9:g.154373341G>A NCBI36
NG_008692.2:g.59354G>A , LRG_254:g.59354G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.828G>A ENSP00000426535.3:p.Gln276=
ENST00000459904.2:n.634G>A
ENST00000498722.3:n.618G>A
ENST00000682650.1:c.1386G>A ENSP00000506904.1:p.Gln462=
ENST00000683032.1:c.1386G>A ENSP00000506771.1:p.Gln462=
ENST00000684195.1:c.1386G>A ENSP00000508220.1:p.Gln462=
ENST00000361308.9:c.1386G>A ENSP00000355292.6:p.Gln462=
ENST00000368300.9:c.1386G>A MANE Select ENSP00000357283.4:p.Gln462=
ENST00000496738.6:n.1761G>A
ENST00000674518.1:c.*736G>A ENSP00000502261.1:n.*736G>A
ENST00000674600.1:c.*1185G>A ENSP00000501666.1:n.*1185G>A
ENST00000674720.1:c.1499G>A ENSP00000502798.1:p.Ser500Asn
ENST00000675431.1:n.1079G>A
ENST00000675455.1:c.*1186G>A ENSP00000501795.1:n.*1186G>A
ENST00000675667.1:c.1386G>A ENSP00000501803.1:p.Gln462=
ENST00000675874.1:c.*857G>A ENSP00000501851.1:n.*857G>A
ENST00000675881.1:c.*397G>A ENSP00000501670.1:n.*397G>A
ENST00000675939.1:c.1386G>A ENSP00000502256.1:p.Gln462=
ENST00000675989.1:n.2245G>A
ENST00000676208.1:c.*489G>A ENSP00000502468.1:n.*489G>A
ENST00000676283.1:n.1761G>A
ENST00000676385.2:c.1386G>A ENSP00000502091.1:p.Gln462=
ENST00000676434.1:c.*397G>A ENSP00000501648.1:n.*397G>A
ENST00000677389.1:c.1386G>A MANE Plus Clinical ENSP00000503633.1:p.Gln462=
ENST00000347559.6:c.1386G>A ENSP00000292304.3:p.Gln462=
ENST00000361308.8:c.1312-265G>A ENSP00000355292.5:n.1312-265G>A
ENST00000368297.5:c.1143G>A ENSP00000357280.1:p.Gln381=
ENST00000368298.2:n.1134G>A
ENST00000368299.7:c.1386G>A ENSP00000357282.3:p.Gln462=
ENST00000368300.8:c.1386G>A ENSP00000357283.4:p.Gln462=
ENST00000368301.6:c.1386G>A ENSP00000357284.2:p.Gln462=
ENST00000448611.6:c.1050G>A ENSP00000395597.2:p.Gln350=
ENST00000459904.1:n.634G>A
ENST00000473598.6:c.1089G>A ENSP00000421821.1:p.Gln363=
ENST00000496738.5:n.771G>A
ENST00000498722.2:n.618G>A
ENST00000508500.1:c.264G>A ENSP00000424977.1:p.Gln88=
NM_001257374.2:c.1050G>A NP_001244303.1:p.Gln350=
NM_001282624.1:c.1143G>A NP_001269553.1:p.Gln381=
NM_001282625.1:c.1386G>A NP_001269554.1:p.Gln462=
NM_001282626.1:c.1386G>A NP_001269555.1:p.Gln462=
NM_005572.3:c.1386G>A , LRG_254t1:c.1386G>A NP_005563.1:p.Gln462=
NM_170707.3:c.1386G>A NP_733821.1:p.Gln462=
NM_170708.3:c.1386G>A NP_733822.1:p.Gln462=
XM_011509533.1:c.1050G>A XP_011507835.1:p.Gln350=
XM_011509534.1:c.762G>A XP_011507836.1:p.Gln254=
XR_921781.1:n.1675G>A
XM_011509534.2:c.762G>A XP_011507836.1:p.Gln254=
XR_921781.2:n.1673G>A
NM_170707.4:c.1386G>A MANE Select NP_733821.1:p.Gln462=
NM_001257374.3:c.1050G>A NP_001244303.1:p.Gln350=
NM_001282626.2:c.1386G>A NP_001269555.1:p.Gln462=
NM_001282624.2:c.1143G>A NP_001269553.1:p.Gln381=
NM_001282625.2:c.1386G>A NP_001269554.1:p.Gln462=
NM_005572.4:c.1386G>A MANE Plus Clinical NP_005563.1:p.Gln462=
NM_170708.4:c.1386G>A NP_733822.1:p.Gln462=