Canonical Allele Identifier: CA342828061

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156108516T>C (hg19) ; chr1:g.156138725T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138725T>C , CM000663.2:g.156138725T>C	GRCh38
NC_000001.10:g.156108516T>C , CM000663.1:g.156108516T>C	GRCh37
NC_000001.9:g.154375140T>C	NCBI36
NG_008692.2:g.61153T>C , LRG_254:g.61153T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000504687.7:c.1378T>C	ENSP00000426535.3:p.Tyr460His
ENST00000682650.1:c.1846T>C	ENSP00000506904.1:p.Tyr616His
ENST00000683032.1:c.1936T>C	ENSP00000506771.1:p.Tyr646His
ENST00000683773.1:n.163+118T>C
ENST00000684195.1:c.*1028T>C	ENSP00000508220.1:n.*1028T>C
ENST00000361308.9:c.1936T>C	ENSP00000355292.6:p.Tyr646His
ENST00000368300.9:c.1936T>C MANE Select	ENSP00000357283.4:p.Tyr646His
ENST00000674518.1:c.*1286T>C	ENSP00000502261.1:n.*1286T>C
ENST00000674600.1:c.*1735T>C	ENSP00000501666.1:n.*1735T>C
ENST00000675455.1:c.*1736T>C	ENSP00000501795.1:n.*1736T>C
ENST00000675667.1:c.1936T>C	ENSP00000501803.1:p.Tyr646His
ENST00000675874.1:c.*1407T>C	ENSP00000501851.1:n.*1407T>C
ENST00000675881.1:c.*947T>C	ENSP00000501670.1:n.*947T>C
ENST00000675939.1:c.1936T>C	ENSP00000502256.1:p.Tyr646His
ENST00000675989.1:n.3539T>C
ENST00000676208.1:c.*1039T>C	ENSP00000502468.1:n.*1039T>C
ENST00000676385.2:c.1846T>C	ENSP00000502091.1:p.Tyr616His
ENST00000676434.1:c.*1691T>C	ENSP00000501648.1:n.*1691T>C
ENST00000347559.6:c.1846T>C	ENSP00000292304.3:p.Tyr616His
ENST00000368299.7:c.1818+118T>C	ENSP00000357282.3:n.1818+118T>C
ENST00000368300.8:c.1936T>C	ENSP00000357283.4:p.Tyr646His
ENST00000448611.6:c.1600T>C	ENSP00000395597.2:p.Tyr534His
ENST00000473598.6:c.1639T>C	ENSP00000421821.1:p.Tyr547His
ENST00000496738.5:n.2149T>C
ENST00000506981.1:n.520T>C
ENST00000508500.1:c.724T>C	ENSP00000424977.1:p.Tyr242His
NM_001257374.2:c.1600T>C	NP_001244303.1:p.Tyr534His
NM_001282626.1:c.1818+118T>C	NP_001269555.1:n.1818+118T>C
NM_170707.3:c.1936T>C	NP_733821.1:p.Tyr646His
NM_170708.3:c.1846T>C	NP_733822.1:p.Tyr616His
XM_011509533.1:c.1600T>C	XP_011507835.1:p.Tyr534His
XM_011509534.1:c.1312T>C	XP_011507836.1:p.Tyr438His
XR_921781.1:n.2225T>C
XM_011509534.2:c.1312T>C	XP_011507836.1:p.Tyr438His
XR_921781.2:n.2223T>C
NM_170707.4:c.1936T>C MANE Select	NP_733821.1:p.Tyr646His
NM_001257374.3:c.1600T>C	NP_001244303.1:p.Tyr534His
NM_001282626.2:c.1818+118T>C	NP_001269555.1:n.1818+118T>C
NM_170708.4:c.1846T>C	NP_733822.1:p.Tyr616His