Canonical Allele Identifier: CA342827867

Gene: LMNA

Linked Data

• gnomAD v4: 1-156138702-G-A
• MyVariant Identifiers: chr1:g.156108493G>A (hg19) ; chr1:g.156138702G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138702G>A , CM000663.2:g.156138702G>A	GRCh38
NC_000001.10:g.156108493G>A , CM000663.1:g.156108493G>A	GRCh37
NC_000001.9:g.154375117G>A	NCBI36
NG_008692.2:g.61130G>A , LRG_254:g.61130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1355G>A	ENSP00000426535.3:p.Gly452Glu
ENST00000682650.1:c.1823G>A	ENSP00000506904.1:p.Gly608Glu
ENST00000683032.1:c.1913G>A	ENSP00000506771.1:p.Gly638Glu
ENST00000683773.1:n.163+95G>A
ENST00000684195.1:c.*1005G>A	ENSP00000508220.1:n.*1005G>A
ENST00000361308.9:c.1913G>A	ENSP00000355292.6:p.Gly638Glu
ENST00000368300.9:c.1913G>A MANE Select	ENSP00000357283.4:p.Gly638Glu
ENST00000674518.1:c.*1263G>A	ENSP00000502261.1:n.*1263G>A
ENST00000674600.1:c.*1712G>A	ENSP00000501666.1:n.*1712G>A
ENST00000675455.1:c.*1713G>A	ENSP00000501795.1:n.*1713G>A
ENST00000675667.1:c.1913G>A	ENSP00000501803.1:p.Gly638Glu
ENST00000675874.1:c.*1384G>A	ENSP00000501851.1:n.*1384G>A
ENST00000675881.1:c.*924G>A	ENSP00000501670.1:n.*924G>A
ENST00000675939.1:c.1913G>A	ENSP00000502256.1:p.Gly638Glu
ENST00000675989.1:n.3516G>A
ENST00000676208.1:c.*1016G>A	ENSP00000502468.1:n.*1016G>A
ENST00000676385.2:c.1823G>A	ENSP00000502091.1:p.Gly608Glu
ENST00000676434.1:c.*1668G>A	ENSP00000501648.1:n.*1668G>A
ENST00000347559.6:c.1823G>A	ENSP00000292304.3:p.Gly608Glu
ENST00000368299.7:c.1818+95G>A	ENSP00000357282.3:n.1818+95G>A
ENST00000368300.8:c.1913G>A	ENSP00000357283.4:p.Gly638Glu
ENST00000448611.6:c.1577G>A	ENSP00000395597.2:p.Gly526Glu
ENST00000473598.6:c.1616G>A	ENSP00000421821.1:p.Gly539Glu
ENST00000496738.5:n.2126G>A
ENST00000506981.1:n.497G>A
ENST00000508500.1:c.701G>A	ENSP00000424977.1:p.Gly234Glu
NM_001257374.2:c.1577G>A	NP_001244303.1:p.Gly526Glu
NM_001282626.1:c.1818+95G>A	NP_001269555.1:n.1818+95G>A
NM_170707.3:c.1913G>A	NP_733821.1:p.Gly638Glu
NM_170708.3:c.1823G>A	NP_733822.1:p.Gly608Glu
XM_011509533.1:c.1577G>A	XP_011507835.1:p.Gly526Glu
XM_011509534.1:c.1289G>A	XP_011507836.1:p.Gly430Glu
XR_921781.1:n.2202G>A
XM_011509534.2:c.1289G>A	XP_011507836.1:p.Gly430Glu
XR_921781.2:n.2200G>A
NM_170707.4:c.1913G>A MANE Select	NP_733821.1:p.Gly638Glu
NM_001257374.3:c.1577G>A	NP_001244303.1:p.Gly526Glu
NM_001282626.2:c.1818+95G>A	NP_001269555.1:n.1818+95G>A
NM_170708.4:c.1823G>A	NP_733822.1:p.Gly608Glu