Canonical Allele Identifier: CA342820565

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156105885G>C (hg19) ; chr1:g.156136094G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156136094G>C , CM000663.2:g.156136094G>C	GRCh38
NC_000001.10:g.156105885G>C , CM000663.1:g.156105885G>C	GRCh37
NC_000001.9:g.154372509G>C	NCBI36
NG_008692.2:g.58522G>C , LRG_254:g.58522G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.572G>C	ENSP00000426535.3:p.Arg191Pro
ENST00000498722.3:n.362G>C
ENST00000682650.1:c.1130G>C	ENSP00000506904.1:p.Arg377Pro
ENST00000683032.1:c.1130G>C	ENSP00000506771.1:p.Arg377Pro
ENST00000684195.1:c.1130G>C	ENSP00000508220.1:p.Arg377Pro
ENST00000361308.9:c.1130G>C	ENSP00000355292.6:p.Arg377Pro
ENST00000368300.9:c.1130G>C MANE Select	ENSP00000357283.4:p.Arg377Pro
ENST00000496738.6:n.1505G>C
ENST00000674518.1:c.*480G>C	ENSP00000502261.1:n.*480G>C
ENST00000674600.1:c.*929G>C	ENSP00000501666.1:n.*929G>C
ENST00000674720.1:c.1130G>C	ENSP00000502798.1:p.Arg377Pro
ENST00000675431.1:n.823G>C
ENST00000675455.1:c.*930G>C	ENSP00000501795.1:n.*930G>C
ENST00000675667.1:c.1130G>C	ENSP00000501803.1:p.Arg377Pro
ENST00000675874.1:c.*601G>C	ENSP00000501851.1:n.*601G>C
ENST00000675881.1:c.*141G>C	ENSP00000501670.1:n.*141G>C
ENST00000675939.1:c.1130G>C	ENSP00000502256.1:p.Arg377Pro
ENST00000675989.1:n.1505G>C
ENST00000676208.1:c.*141G>C	ENSP00000502468.1:n.*141G>C
ENST00000676283.1:n.1505G>C
ENST00000676385.2:c.1130G>C	ENSP00000502091.1:p.Arg377Pro
ENST00000676434.1:c.*141G>C	ENSP00000501648.1:n.*141G>C
ENST00000677389.1:c.1130G>C MANE Plus Clinical	ENSP00000503633.1:p.Arg377Pro
ENST00000347559.6:c.1130G>C	ENSP00000292304.3:p.Arg377Pro
ENST00000361308.8:c.1130G>C	ENSP00000355292.5:p.Arg377Pro
ENST00000368297.5:c.887G>C	ENSP00000357280.1:p.Arg296Pro
ENST00000368298.2:n.394G>C
ENST00000368299.7:c.1130G>C	ENSP00000357282.3:p.Arg377Pro
ENST00000368300.8:c.1130G>C	ENSP00000357283.4:p.Arg377Pro
ENST00000368301.6:c.1130G>C	ENSP00000357284.2:p.Arg377Pro
ENST00000448611.6:c.794G>C	ENSP00000395597.2:p.Arg265Pro
ENST00000473598.6:c.833G>C	ENSP00000421821.1:p.Arg278Pro
ENST00000496738.5:n.515G>C
ENST00000498722.2:n.362G>C
ENST00000508500.1:c.8G>C	ENSP00000424977.1:p.Arg3Pro
NM_001257374.2:c.794G>C	NP_001244303.1:p.Arg265Pro
NM_001282624.1:c.887G>C	NP_001269553.1:p.Arg296Pro
NM_001282625.1:c.1130G>C	NP_001269554.1:p.Arg377Pro
NM_001282626.1:c.1130G>C	NP_001269555.1:p.Arg377Pro
NM_005572.3:c.1130G>C , LRG_254t1:c.1130G>C	NP_005563.1:p.Arg377Pro
NM_170707.3:c.1130G>C	NP_733821.1:p.Arg377Pro
NM_170708.3:c.1130G>C	NP_733822.1:p.Arg377Pro
XM_011509533.1:c.794G>C	XP_011507835.1:p.Arg265Pro
XM_011509534.1:c.506G>C	XP_011507836.1:p.Arg169Pro
XR_921781.1:n.1419G>C
XM_011509534.2:c.506G>C	XP_011507836.1:p.Arg169Pro
XR_921781.2:n.1417G>C
NM_170707.4:c.1130G>C MANE Select	NP_733821.1:p.Arg377Pro
NM_001257374.3:c.794G>C	NP_001244303.1:p.Arg265Pro
NM_001282626.2:c.1130G>C	NP_001269555.1:p.Arg377Pro
NM_001282624.2:c.887G>C	NP_001269553.1:p.Arg296Pro
NM_001282625.2:c.1130G>C	NP_001269554.1:p.Arg377Pro
NM_005572.4:c.1130G>C MANE Plus Clinical	NP_005563.1:p.Arg377Pro
NM_170708.4:c.1130G>C	NP_733822.1:p.Arg377Pro