Canonical Allele Identifier: CA1200463842
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156114877C= , CM000663.2:g.156114877C= GRCh38
NC_000001.10:g.156084668C= , CM000663.1:g.156084668C= GRCh37
NC_000001.9:g.154351292C= NCBI36
NG_008692.2:g.37305C= , LRG_254:g.37305C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682650.1:c.-42C= ENSP00000506904.1:n.-42C=
ENST00000683032.1:c.-42C= ENSP00000506771.1:n.-42C=
ENST00000684195.1:c.-42C= ENSP00000508220.1:n.-42C=
ENST00000361308.9:c.-42C= ENSP00000355292.6:n.-42C=
ENST00000368300.9:c.-42C= MANE Select ENSP00000357283.4:n.-42C=
ENST00000496738.6:n.334C=
ENST00000674518.1:c.-42C= ENSP00000502261.1:n.-42C=
ENST00000674600.1:c.-42C= ENSP00000501666.1:n.-42C=
ENST00000674720.1:c.-42C= ENSP00000502798.1:n.-42C=
ENST00000675455.1:c.-42C= ENSP00000501795.1:n.-42C=
ENST00000675667.1:c.-42C= ENSP00000501803.1:n.-42C=
ENST00000675874.1:c.-42C= ENSP00000501851.1:n.-42C=
ENST00000675881.1:c.-42C= ENSP00000501670.1:n.-42C=
ENST00000675939.1:c.-42C= ENSP00000502256.1:n.-42C=
ENST00000675989.1:n.334C=
ENST00000676208.1:c.-42C= ENSP00000502468.1:n.-42C=
ENST00000676283.1:n.334C=
ENST00000676385.2:c.-42C= ENSP00000502091.1:n.-42C=
ENST00000676434.1:c.-42C= ENSP00000501648.1:n.-42C=
ENST00000677389.1:c.-42C= MANE Plus Clinical ENSP00000503633.1:n.-42C=
ENST00000347559.6:c.-42C= ENSP00000292304.3:n.-42C=
ENST00000361308.8:c.-42C= ENSP00000355292.5:n.-42C=
ENST00000368299.7:c.-42C= ENSP00000357282.3:n.-42C=
ENST00000368300.8:c.-42C= ENSP00000357283.4:n.-42C=
ENST00000368301.6:c.-42C= ENSP00000357284.2:n.-42C=
ENST00000469565.6:n.80-87C=
ENST00000470199.2:n.167C=
ENST00000478063.2:n.167C=
ENST00000502751.5:n.329-15740C=
NM_001282625.1:c.-42C= NP_001269554.1:n.-42C=
NM_001282626.1:c.-42C= NP_001269555.1:n.-42C=
NM_005572.3:c.-42C= , LRG_254t1:c.-42C= NP_005563.1:n.-42C=
NM_170707.3:c.-42C= NP_733821.1:n.-42C=
NM_170708.3:c.-42C= NP_733822.1:n.-42C=
XR_921781.1:n.208C=
XR_921781.2:n.206C=
NM_170707.4:c.-42C= MANE Select NP_733821.1:n.-42C=
NM_001282626.2:c.-42C= NP_001269555.1:n.-42C=
NM_001282625.2:c.-42C= NP_001269554.1:n.-42C=
NM_005572.4:c.-42C= MANE Plus Clinical NP_005563.1:n.-42C=
NM_170708.4:c.-42C= NP_733822.1:n.-42C=