Canonical Allele Identifier: CA10607025

Gene: LMNA

Linked Data

• ClinVar Variation Id: 291119
• ClinVar RCV Id: RCV000347929
• dbSNP Id: rs886044657
• MyVariant Identifiers: chr1:g.156106905T>C (hg19) ; chr1:g.156137114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137114T>C , CM000663.2:g.156137114T>C	GRCh38
NC_000001.10:g.156106905T>C , CM000663.1:g.156106905T>C	GRCh37
NC_000001.9:g.154373529T>C	NCBI36
NG_008692.2:g.59542T>C , LRG_254:g.59542T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.932T>C	ENSP00000426535.3:p.Ile311Thr
ENST00000459904.2:n.738T>C
ENST00000498722.3:n.722T>C
ENST00000682650.1:c.1490T>C	ENSP00000506904.1:p.Ile497Thr
ENST00000683032.1:c.1490T>C	ENSP00000506771.1:p.Ile497Thr
ENST00000684195.1:c.1490T>C	ENSP00000508220.1:p.Ile497Thr
ENST00000361308.9:c.1490T>C	ENSP00000355292.6:p.Ile497Thr
ENST00000368300.9:c.1490T>C MANE Select	ENSP00000357283.4:p.Ile497Thr
ENST00000496738.6:n.1949T>C
ENST00000674518.1:c.*840T>C	ENSP00000502261.1:n.*840T>C
ENST00000674600.1:c.*1289T>C	ENSP00000501666.1:n.*1289T>C
ENST00000674720.1:c.*52T>C	ENSP00000502798.1:n.*52T>C
ENST00000675431.1:n.1183T>C
ENST00000675455.1:c.*1290T>C	ENSP00000501795.1:n.*1290T>C
ENST00000675667.1:c.1490T>C	ENSP00000501803.1:p.Ile497Thr
ENST00000675874.1:c.*961T>C	ENSP00000501851.1:n.*961T>C
ENST00000675881.1:c.*501T>C	ENSP00000501670.1:n.*501T>C
ENST00000675939.1:c.1490T>C	ENSP00000502256.1:p.Ile497Thr
ENST00000675989.1:n.2349T>C
ENST00000676208.1:c.*593T>C	ENSP00000502468.1:n.*593T>C
ENST00000676283.1:n.1865T>C
ENST00000676385.2:c.1490T>C	ENSP00000502091.1:p.Ile497Thr
ENST00000676434.1:c.*501T>C	ENSP00000501648.1:n.*501T>C
ENST00000677389.1:c.1490T>C MANE Plus Clinical	ENSP00000503633.1:p.Ile497Thr
ENST00000347559.6:c.1490T>C	ENSP00000292304.3:p.Ile497Thr
ENST00000361308.8:c.1312-77T>C	ENSP00000355292.5:n.1312-77T>C
ENST00000368297.5:c.1247T>C	ENSP00000357280.1:p.Ile416Thr
ENST00000368298.2:n.1322T>C
ENST00000368299.7:c.1490T>C	ENSP00000357282.3:p.Ile497Thr
ENST00000368300.8:c.1490T>C	ENSP00000357283.4:p.Ile497Thr
ENST00000368301.6:c.1490T>C	ENSP00000357284.2:p.Ile497Thr
ENST00000448611.6:c.1154T>C	ENSP00000395597.2:p.Ile385Thr
ENST00000459904.1:n.738T>C
ENST00000473598.6:c.1193T>C	ENSP00000421821.1:p.Ile398Thr
ENST00000496738.5:n.959T>C
ENST00000498722.2:n.722T>C
ENST00000508500.1:c.368T>C	ENSP00000424977.1:p.Ile123Thr
NM_001257374.2:c.1154T>C	NP_001244303.1:p.Ile385Thr
NM_001282624.1:c.1247T>C	NP_001269553.1:p.Ile416Thr
NM_001282625.1:c.1490T>C	NP_001269554.1:p.Ile497Thr
NM_001282626.1:c.1490T>C	NP_001269555.1:p.Ile497Thr
NM_005572.3:c.1490T>C , LRG_254t1:c.1490T>C	NP_005563.1:p.Ile497Thr
NM_170707.3:c.1490T>C	NP_733821.1:p.Ile497Thr
NM_170708.3:c.1490T>C	NP_733822.1:p.Ile497Thr
XM_011509533.1:c.1154T>C	XP_011507835.1:p.Ile385Thr
XM_011509534.1:c.866T>C	XP_011507836.1:p.Ile289Thr
XR_921781.1:n.1779T>C
XM_011509534.2:c.866T>C	XP_011507836.1:p.Ile289Thr
XR_921781.2:n.1777T>C
NM_170707.4:c.1490T>C MANE Select	NP_733821.1:p.Ile497Thr
NM_001257374.3:c.1154T>C	NP_001244303.1:p.Ile385Thr
NM_001282626.2:c.1490T>C	NP_001269555.1:p.Ile497Thr
NM_001282624.2:c.1247T>C	NP_001269553.1:p.Ile416Thr
NM_001282625.2:c.1490T>C	NP_001269554.1:p.Ile497Thr
NM_005572.4:c.1490T>C MANE Plus Clinical	NP_005563.1:p.Ile497Thr
NM_170708.4:c.1490T>C	NP_733822.1:p.Ile497Thr