Canonical Allele Identifier: CA421257565

Gene: LMNA

Linked Data

• gnomAD v4: 1-156134813-T-C
• MyVariant Identifiers: chr1:g.156104604T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134813T>C , CM000663.2:g.156134813T>C	GRCh38
NC_000001.10:g.156104604T>C , CM000663.1:g.156104604T>C	GRCh37
NC_000001.9:g.154371228T>C	NCBI36
NG_008692.2:g.57241T>C , LRG_254:g.57241T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.90T>C	ENSP00000426535.3:p.Arg30=
ENST00000682650.1:c.648T>C	ENSP00000506904.1:p.Arg216=
ENST00000683032.1:c.648T>C	ENSP00000506771.1:p.Arg216=
ENST00000684195.1:c.648T>C	ENSP00000508220.1:p.Arg216=
ENST00000361308.9:c.648T>C	ENSP00000355292.6:p.Arg216=
ENST00000368300.9:c.648T>C MANE Select	ENSP00000357283.4:p.Arg216=
ENST00000496738.6:n.1023T>C
ENST00000504687.6:c.-17T>C	ENSP00000426535.2:n.-17T>C
ENST00000674518.1:c.643T>C	ENSP00000502261.1:p.Ter215Arg
ENST00000674600.1:c.*447T>C	ENSP00000501666.1:n.*447T>C
ENST00000674720.1:c.648T>C	ENSP00000502798.1:p.Arg216=
ENST00000675431.1:n.341T>C
ENST00000675455.1:c.*448T>C	ENSP00000501795.1:n.*448T>C
ENST00000675667.1:c.648T>C	ENSP00000501803.1:p.Arg216=
ENST00000675874.1:c.*119T>C	ENSP00000501851.1:n.*119T>C
ENST00000675881.1:c.648T>C	ENSP00000501670.1:p.Arg216=
ENST00000675939.1:c.648T>C	ENSP00000502256.1:p.Arg216=
ENST00000675989.1:n.1023T>C
ENST00000676208.1:c.648T>C	ENSP00000502468.1:p.Arg216=
ENST00000676283.1:n.1023T>C
ENST00000676385.2:c.648T>C	ENSP00000502091.1:p.Arg216=
ENST00000676434.1:c.648T>C	ENSP00000501648.1:p.Arg216=
ENST00000677389.1:c.648T>C MANE Plus Clinical	ENSP00000503633.1:p.Arg216=
ENST00000347559.6:c.648T>C	ENSP00000292304.3:p.Arg216=
ENST00000361308.8:c.648T>C	ENSP00000355292.5:p.Arg216=
ENST00000368297.5:c.405T>C	ENSP00000357280.1:p.Arg135=
ENST00000368299.7:c.648T>C	ENSP00000357282.3:p.Arg216=
ENST00000368300.8:c.648T>C	ENSP00000357283.4:p.Arg216=
ENST00000368301.6:c.648T>C	ENSP00000357284.2:p.Arg216=
ENST00000448611.6:c.312T>C	ENSP00000395597.2:p.Arg104=
ENST00000473598.6:c.351T>C	ENSP00000421821.1:p.Arg117=
ENST00000504687.5:c.399T>C	ENSP00000426535.1:p.Arg133=
ENST00000515459.5:c.*322T>C	ENSP00000424518.1:n.*322T>C
ENST00000515824.1:n.9T>C
NM_001257374.2:c.312T>C	NP_001244303.1:p.Arg104=
NM_001282624.1:c.405T>C	NP_001269553.1:p.Arg135=
NM_001282625.1:c.648T>C	NP_001269554.1:p.Arg216=
NM_001282626.1:c.648T>C	NP_001269555.1:p.Arg216=
NM_005572.3:c.648T>C , LRG_254t1:c.648T>C	NP_005563.1:p.Arg216=
NM_170707.3:c.648T>C	NP_733821.1:p.Arg216=
NM_170708.3:c.648T>C	NP_733822.1:p.Arg216=
XM_011509533.1:c.312T>C	XP_011507835.1:p.Arg104=
XM_011509534.1:c.-17T>C	XP_011507836.1:n.-17T>C
XR_921781.1:n.897T>C
XM_011509534.2:c.-17T>C	XP_011507836.1:n.-17T>C
XR_921781.2:n.895T>C
NM_170707.4:c.648T>C MANE Select	NP_733821.1:p.Arg216=
NM_001257374.3:c.312T>C	NP_001244303.1:p.Arg104=
NM_001282626.2:c.648T>C	NP_001269555.1:p.Arg216=
NM_001282624.2:c.405T>C	NP_001269553.1:p.Arg135=
NM_001282625.2:c.648T>C	NP_001269554.1:p.Arg216=
NM_005572.4:c.648T>C MANE Plus Clinical	NP_005563.1:p.Arg216=
NM_170708.4:c.648T>C	NP_733822.1:p.Arg216=