Canonical Allele Identifier: CA342827800

Gene: LMNA

Linked Data

• gnomAD v4: 1-156138696-G-C
• MyVariant Identifiers: chr1:g.156108487G>C (hg19) ; chr1:g.156138696G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138696G>C , CM000663.2:g.156138696G>C	GRCh38
NC_000001.10:g.156108487G>C , CM000663.1:g.156108487G>C	GRCh37
NC_000001.9:g.154375111G>C	NCBI36
NG_008692.2:g.61124G>C , LRG_254:g.61124G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1349G>C	ENSP00000426535.3:p.Ser450Thr
ENST00000682650.1:c.1817G>C	ENSP00000506904.1:p.Ser606Thr
ENST00000683032.1:c.1907G>C	ENSP00000506771.1:p.Ser636Thr
ENST00000683773.1:n.163+89G>C
ENST00000684195.1:c.*999G>C	ENSP00000508220.1:n.*999G>C
ENST00000361308.9:c.1907G>C	ENSP00000355292.6:p.Ser636Thr
ENST00000368300.9:c.1907G>C MANE Select	ENSP00000357283.4:p.Ser636Thr
ENST00000674518.1:c.*1257G>C	ENSP00000502261.1:n.*1257G>C
ENST00000674600.1:c.*1706G>C	ENSP00000501666.1:n.*1706G>C
ENST00000675455.1:c.*1707G>C	ENSP00000501795.1:n.*1707G>C
ENST00000675667.1:c.1907G>C	ENSP00000501803.1:p.Ser636Thr
ENST00000675874.1:c.*1378G>C	ENSP00000501851.1:n.*1378G>C
ENST00000675881.1:c.*918G>C	ENSP00000501670.1:n.*918G>C
ENST00000675939.1:c.1907G>C	ENSP00000502256.1:p.Ser636Thr
ENST00000675989.1:n.3510G>C
ENST00000676208.1:c.*1010G>C	ENSP00000502468.1:n.*1010G>C
ENST00000676385.2:c.1817G>C	ENSP00000502091.1:p.Ser606Thr
ENST00000676434.1:c.*1662G>C	ENSP00000501648.1:n.*1662G>C
ENST00000347559.6:c.1817G>C	ENSP00000292304.3:p.Ser606Thr
ENST00000368299.7:c.1818+89G>C	ENSP00000357282.3:n.1818+89G>C
ENST00000368300.8:c.1907G>C	ENSP00000357283.4:p.Ser636Thr
ENST00000448611.6:c.1571G>C	ENSP00000395597.2:p.Ser524Thr
ENST00000473598.6:c.1610G>C	ENSP00000421821.1:p.Ser537Thr
ENST00000496738.5:n.2120G>C
ENST00000506981.1:n.491G>C
ENST00000508500.1:c.695G>C	ENSP00000424977.1:p.Ser232Thr
NM_001257374.2:c.1571G>C	NP_001244303.1:p.Ser524Thr
NM_001282626.1:c.1818+89G>C	NP_001269555.1:n.1818+89G>C
NM_170707.3:c.1907G>C	NP_733821.1:p.Ser636Thr
NM_170708.3:c.1817G>C	NP_733822.1:p.Ser606Thr
XM_011509533.1:c.1571G>C	XP_011507835.1:p.Ser524Thr
XM_011509534.1:c.1283G>C	XP_011507836.1:p.Ser428Thr
XR_921781.1:n.2196G>C
XM_011509534.2:c.1283G>C	XP_011507836.1:p.Ser428Thr
XR_921781.2:n.2194G>C
NM_170707.4:c.1907G>C MANE Select	NP_733821.1:p.Ser636Thr
NM_001257374.3:c.1571G>C	NP_001244303.1:p.Ser524Thr
NM_001282626.2:c.1818+89G>C	NP_001269555.1:n.1818+89G>C
NM_170708.4:c.1817G>C	NP_733822.1:p.Ser606Thr