Canonical Allele Identifier: CA1008052352
Gene: LMNA HGNC NCBI

Linked Data

dbSNP Id: rs1649686263

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156114847T>G , CM000663.2:g.156114847T>G GRCh38
NC_000001.10:g.156084638T>G , CM000663.1:g.156084638T>G GRCh37
NC_000001.9:g.154351262T>G NCBI36
NG_008692.2:g.37275T>G , LRG_254:g.37275T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682650.1:c.-72T>G ENSP00000506904.1:n.-72T>G
ENST00000683032.1:c.-72T>G ENSP00000506771.1:n.-72T>G
ENST00000684195.1:c.-72T>G ENSP00000508220.1:n.-72T>G
ENST00000361308.9:c.-72T>G ENSP00000355292.6:n.-72T>G
ENST00000368300.9:c.-72T>G MANE Select ENSP00000357283.4:n.-72T>G
ENST00000496738.6:n.304T>G
ENST00000674518.1:c.-72T>G ENSP00000502261.1:n.-72T>G
ENST00000674600.1:c.-72T>G ENSP00000501666.1:n.-72T>G
ENST00000674720.1:c.-72T>G ENSP00000502798.1:n.-72T>G
ENST00000675455.1:c.-72T>G ENSP00000501795.1:n.-72T>G
ENST00000675667.1:c.-72T>G ENSP00000501803.1:n.-72T>G
ENST00000675874.1:c.-72T>G ENSP00000501851.1:n.-72T>G
ENST00000675881.1:c.-72T>G ENSP00000501670.1:n.-72T>G
ENST00000675939.1:c.-72T>G ENSP00000502256.1:n.-72T>G
ENST00000675989.1:n.304T>G
ENST00000676208.1:c.-72T>G ENSP00000502468.1:n.-72T>G
ENST00000676283.1:n.304T>G
ENST00000676385.2:c.-72T>G ENSP00000502091.1:n.-72T>G
ENST00000676434.1:c.-72T>G ENSP00000501648.1:n.-72T>G
ENST00000677389.1:c.-72T>G MANE Plus Clinical ENSP00000503633.1:n.-72T>G
ENST00000347559.6:c.-72T>G ENSP00000292304.3:n.-72T>G
ENST00000361308.8:c.-72T>G ENSP00000355292.5:n.-72T>G
ENST00000368299.7:c.-72T>G ENSP00000357282.3:n.-72T>G
ENST00000368300.8:c.-72T>G ENSP00000357283.4:n.-72T>G
ENST00000368301.6:c.-72T>G ENSP00000357284.2:n.-72T>G
ENST00000469565.6:n.79+56T>G
ENST00000470199.2:n.137T>G
ENST00000478063.2:n.137T>G
ENST00000502751.5:n.329-15770T>G
NM_001282625.1:c.-72T>G NP_001269554.1:n.-72T>G
NM_001282626.1:c.-72T>G NP_001269555.1:n.-72T>G
NM_005572.3:c.-72T>G , LRG_254t1:c.-72T>G NP_005563.1:n.-72T>G
NM_170707.3:c.-72T>G NP_733821.1:n.-72T>G
NM_170708.3:c.-72T>G NP_733822.1:n.-72T>G
XR_921781.1:n.178T>G
XR_921781.2:n.176T>G
NM_170707.4:c.-72T>G MANE Select NP_733821.1:n.-72T>G
NM_001282626.2:c.-72T>G NP_001269555.1:n.-72T>G
NM_001282625.2:c.-72T>G NP_001269554.1:n.-72T>G
NM_005572.4:c.-72T>G MANE Plus Clinical NP_005563.1:n.-72T>G
NM_170708.4:c.-72T>G NP_733822.1:n.-72T>G