Canonical Allele Identifier: CA2648353397

Gene: LMNA

Linked Data

• gnomAD v4: 1-156138419-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138419G>A , CM000663.2:g.156138419G>A	GRCh38
NC_000001.10:g.156108210G>A , CM000663.1:g.156108210G>A	GRCh37
NC_000001.9:g.154374834G>A	NCBI36
NG_008692.2:g.60847G>A , LRG_254:g.60847G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1141-69G>A	ENSP00000426535.3:n.1141-69G>A
ENST00000682650.1:c.1609-69G>A	ENSP00000506904.1:n.1609-69G>A
ENST00000683032.1:c.1699-69G>A	ENSP00000506771.1:n.1699-69G>A
ENST00000683773.1:n.44-69G>A
ENST00000684195.1:c.*722G>A	ENSP00000508220.1:n.*722G>A
ENST00000361308.9:c.1699-69G>A	ENSP00000355292.6:n.1699-69G>A
ENST00000368300.9:c.1699-69G>A MANE Select	ENSP00000357283.4:n.1699-69G>A
ENST00000496738.6:n.2833G>A
ENST00000674518.1:c.*1049-69G>A	ENSP00000502261.1:n.*1049-69G>A
ENST00000674600.1:c.*1498-69G>A	ENSP00000501666.1:n.*1498-69G>A
ENST00000674720.1:c.*936G>A	ENSP00000502798.1:n.*936G>A
ENST00000675455.1:c.*1499-69G>A	ENSP00000501795.1:n.*1499-69G>A
ENST00000675667.1:c.1699-69G>A	ENSP00000501803.1:n.1699-69G>A
ENST00000675874.1:c.*1170-69G>A	ENSP00000501851.1:n.*1170-69G>A
ENST00000675881.1:c.*710-69G>A	ENSP00000501670.1:n.*710-69G>A
ENST00000675939.1:c.1699-69G>A	ENSP00000502256.1:n.1699-69G>A
ENST00000675989.1:n.3233G>A
ENST00000676208.1:c.*802-69G>A	ENSP00000502468.1:n.*802-69G>A
ENST00000676283.1:n.3170G>A
ENST00000676385.2:c.1609-69G>A	ENSP00000502091.1:n.1609-69G>A
ENST00000676434.1:c.*1385G>A	ENSP00000501648.1:n.*1385G>A
ENST00000347559.6:c.1609-69G>A	ENSP00000292304.3:n.1609-69G>A
ENST00000368299.7:c.1699-69G>A	ENSP00000357282.3:n.1699-69G>A
ENST00000368300.8:c.1699-69G>A	ENSP00000357283.4:n.1699-69G>A
ENST00000448611.6:c.1363-69G>A	ENSP00000395597.2:n.1363-69G>A
ENST00000473598.6:c.1402-69G>A	ENSP00000421821.1:n.1402-69G>A
ENST00000496738.5:n.1843G>A
ENST00000506981.1:n.283-69G>A
ENST00000508500.1:c.487-69G>A	ENSP00000424977.1:n.487-69G>A
NM_001257374.2:c.1363-69G>A	NP_001244303.1:n.1363-69G>A
NM_001282626.1:c.1699-69G>A	NP_001269555.1:n.1699-69G>A
NM_170707.3:c.1699-69G>A	NP_733821.1:n.1699-69G>A
NM_170708.3:c.1609-69G>A	NP_733822.1:n.1609-69G>A
XM_011509533.1:c.1363-69G>A	XP_011507835.1:n.1363-69G>A
XM_011509534.1:c.1075-69G>A	XP_011507836.1:n.1075-69G>A
XR_921781.1:n.1988-69G>A
XM_011509534.2:c.1075-69G>A	XP_011507836.1:n.1075-69G>A
XR_921781.2:n.1986-69G>A
NM_170707.4:c.1699-69G>A MANE Select	NP_733821.1:n.1699-69G>A
NM_001257374.3:c.1363-69G>A	NP_001244303.1:n.1363-69G>A
NM_001282626.2:c.1699-69G>A	NP_001269555.1:n.1699-69G>A
NM_170708.4:c.1609-69G>A	NP_733822.1:n.1609-69G>A