Canonical Allele Identifier: CA342827270

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156108423T>A (hg19) ; chr1:g.156138632T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138632T>A , CM000663.2:g.156138632T>A	GRCh38
NC_000001.10:g.156108423T>A , CM000663.1:g.156108423T>A	GRCh37
NC_000001.9:g.154375047T>A	NCBI36
NG_008692.2:g.61060T>A , LRG_254:g.61060T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1285T>A	ENSP00000426535.3:p.Ser429Thr
ENST00000682650.1:c.1753T>A	ENSP00000506904.1:p.Ser585Thr
ENST00000683032.1:c.1843T>A	ENSP00000506771.1:p.Ser615Thr
ENST00000683773.1:n.163+25T>A
ENST00000684195.1:c.*935T>A	ENSP00000508220.1:n.*935T>A
ENST00000361308.9:c.1843T>A	ENSP00000355292.6:p.Ser615Thr
ENST00000368300.9:c.1843T>A MANE Select	ENSP00000357283.4:p.Ser615Thr
ENST00000674518.1:c.*1193T>A	ENSP00000502261.1:n.*1193T>A
ENST00000674600.1:c.*1642T>A	ENSP00000501666.1:n.*1642T>A
ENST00000675455.1:c.*1643T>A	ENSP00000501795.1:n.*1643T>A
ENST00000675667.1:c.1843T>A	ENSP00000501803.1:p.Ser615Thr
ENST00000675874.1:c.*1314T>A	ENSP00000501851.1:n.*1314T>A
ENST00000675881.1:c.*854T>A	ENSP00000501670.1:n.*854T>A
ENST00000675939.1:c.1843T>A	ENSP00000502256.1:p.Ser615Thr
ENST00000675989.1:n.3446T>A
ENST00000676208.1:c.*946T>A	ENSP00000502468.1:n.*946T>A
ENST00000676385.2:c.1753T>A	ENSP00000502091.1:p.Ser585Thr
ENST00000676434.1:c.*1598T>A	ENSP00000501648.1:n.*1598T>A
ENST00000347559.6:c.1753T>A	ENSP00000292304.3:p.Ser585Thr
ENST00000368299.7:c.1818+25T>A	ENSP00000357282.3:n.1818+25T>A
ENST00000368300.8:c.1843T>A	ENSP00000357283.4:p.Ser615Thr
ENST00000448611.6:c.1507T>A	ENSP00000395597.2:p.Ser503Thr
ENST00000473598.6:c.1546T>A	ENSP00000421821.1:p.Ser516Thr
ENST00000496738.5:n.2056T>A
ENST00000506981.1:n.427T>A
ENST00000508500.1:c.631T>A	ENSP00000424977.1:p.Ser211Thr
NM_001257374.2:c.1507T>A	NP_001244303.1:p.Ser503Thr
NM_001282626.1:c.1818+25T>A	NP_001269555.1:n.1818+25T>A
NM_170707.3:c.1843T>A	NP_733821.1:p.Ser615Thr
NM_170708.3:c.1753T>A	NP_733822.1:p.Ser585Thr
XM_011509533.1:c.1507T>A	XP_011507835.1:p.Ser503Thr
XM_011509534.1:c.1219T>A	XP_011507836.1:p.Ser407Thr
XR_921781.1:n.2132T>A
XM_011509534.2:c.1219T>A	XP_011507836.1:p.Ser407Thr
XR_921781.2:n.2130T>A
NM_170707.4:c.1843T>A MANE Select	NP_733821.1:p.Ser615Thr
NM_001257374.3:c.1507T>A	NP_001244303.1:p.Ser503Thr
NM_001282626.2:c.1818+25T>A	NP_001269555.1:n.1818+25T>A
NM_170708.4:c.1753T>A	NP_733822.1:p.Ser585Thr