Canonical Allele Identifier: CA2648352012

Gene: LMNA

Linked Data

• gnomAD v4: 1-156137875-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156137875C>G , CM000663.2:g.156137875C>G	GRCh38
NC_000001.10:g.156107666C>G , CM000663.1:g.156107666C>G	GRCh37
NC_000001.9:g.154374290C>G	NCBI36
NG_008692.2:g.60303C>G , LRG_254:g.60303C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1140+132C>G	ENSP00000426535.3:n.1140+132C>G
ENST00000682650.1:c.1609-613C>G	ENSP00000506904.1:n.1609-613C>G
ENST00000683032.1:c.1698+132C>G	ENSP00000506771.1:n.1698+132C>G
ENST00000683773.1:n.43+132C>G
ENST00000684195.1:c.*178C>G	ENSP00000508220.1:n.*178C>G
ENST00000361308.9:c.1698+132C>G	ENSP00000355292.6:n.1698+132C>G
ENST00000368300.9:c.1698+132C>G MANE Select	ENSP00000357283.4:n.1698+132C>G
ENST00000496738.6:n.2289C>G
ENST00000674518.1:c.*1048+132C>G	ENSP00000502261.1:n.*1048+132C>G
ENST00000674600.1:c.*1497+132C>G	ENSP00000501666.1:n.*1497+132C>G
ENST00000674720.1:c.*392C>G	ENSP00000502798.1:n.*392C>G
ENST00000675455.1:c.*1498+132C>G	ENSP00000501795.1:n.*1498+132C>G
ENST00000675667.1:c.1698+132C>G	ENSP00000501803.1:n.1698+132C>G
ENST00000675874.1:c.*1169+132C>G	ENSP00000501851.1:n.*1169+132C>G
ENST00000675881.1:c.*709+132C>G	ENSP00000501670.1:n.*709+132C>G
ENST00000675939.1:c.1698+132C>G	ENSP00000502256.1:n.1698+132C>G
ENST00000675989.1:n.2689C>G
ENST00000676208.1:c.*801+132C>G	ENSP00000502468.1:n.*801+132C>G
ENST00000676283.1:n.2626C>G
ENST00000676385.2:c.1609-613C>G	ENSP00000502091.1:n.1609-613C>G
ENST00000676434.1:c.*841C>G	ENSP00000501648.1:n.*841C>G
ENST00000347559.6:c.1609-613C>G	ENSP00000292304.3:n.1609-613C>G
ENST00000368299.7:c.1698+132C>G	ENSP00000357282.3:n.1698+132C>G
ENST00000368300.8:c.1698+132C>G	ENSP00000357283.4:n.1698+132C>G
ENST00000448611.6:c.1362+132C>G	ENSP00000395597.2:n.1362+132C>G
ENST00000473598.6:c.1401+132C>G	ENSP00000421821.1:n.1401+132C>G
ENST00000496738.5:n.1299C>G
ENST00000498722.2:n.1062C>G
ENST00000506981.1:n.282+132C>G
ENST00000508500.1:c.487-613C>G	ENSP00000424977.1:n.487-613C>G
NM_001257374.2:c.1362+132C>G	NP_001244303.1:n.1362+132C>G
NM_001282626.1:c.1698+132C>G	NP_001269555.1:n.1698+132C>G
NM_170707.3:c.1698+132C>G	NP_733821.1:n.1698+132C>G
NM_170708.3:c.1609-613C>G	NP_733822.1:n.1609-613C>G
XM_011509533.1:c.1362+132C>G	XP_011507835.1:n.1362+132C>G
XM_011509534.1:c.1074+132C>G	XP_011507836.1:n.1074+132C>G
XR_921781.1:n.1987+132C>G
XM_011509534.2:c.1074+132C>G	XP_011507836.1:n.1074+132C>G
XR_921781.2:n.1985+132C>G
NM_170707.4:c.1698+132C>G MANE Select	NP_733821.1:n.1698+132C>G
NM_001257374.3:c.1362+132C>G	NP_001244303.1:n.1362+132C>G
NM_001282626.2:c.1698+132C>G	NP_001269555.1:n.1698+132C>G
NM_170708.4:c.1609-613C>G	NP_733822.1:n.1609-613C>G