Canonical Allele Identifier: CA889742117

Gene: LMNA

Linked Data

• dbSNP Id: rs1438292067
• gnomAD v3: 1-156114745-ACCCAGATCCCGAGGTCCGACAGCGCCCGG-A
• gnomAD v4: 1-156114745-ACCCAGATCCCGAGGTCCGACAGCGCCCGG-A
• MyVariant Identifiers: chr1:g.156084537_156084565del (hg19) ; chr1:g.156114746_156114774del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156114756_156114784del , CM000663.2:g.156114756_156114784del	GRCh38
NC_000001.10:g.156084547_156084575del , CM000663.1:g.156084547_156084575del	GRCh37
NC_000001.9:g.154351171_154351199del	NCBI36
NG_008692.2:g.37184_37212del , LRG_254:g.37184_37212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682650.1:c.-163_-135del	ENSP00000506904.1:n.-163_-135del
ENST00000683032.1:c.-163_-135del	ENSP00000506771.1:n.-163_-135del
ENST00000684195.1:c.-163_-135del	ENSP00000508220.1:n.-163_-135del
ENST00000361308.9:c.-163_-135del	ENSP00000355292.6:n.-163_-135del
ENST00000368300.9:c.-163_-135del MANE Select	ENSP00000357283.4:n.-163_-135del
ENST00000496738.6:n.213_241del
ENST00000674518.1:c.-163_-135del	ENSP00000502261.1:n.-163_-135del
ENST00000674600.1:c.-163_-135del	ENSP00000501666.1:n.-163_-135del
ENST00000674720.1:c.-163_-135del	ENSP00000502798.1:n.-163_-135del
ENST00000675455.1:c.-163_-135del	ENSP00000501795.1:n.-163_-135del
ENST00000675667.1:c.-163_-135del	ENSP00000501803.1:n.-163_-135del
ENST00000675874.1:c.-163_-135del	ENSP00000501851.1:n.-163_-135del
ENST00000675881.1:c.-163_-135del	ENSP00000501670.1:n.-163_-135del
ENST00000675939.1:c.-163_-135del	ENSP00000502256.1:n.-163_-135del
ENST00000675989.1:n.213_241del
ENST00000676208.1:c.-163_-135del	ENSP00000502468.1:n.-163_-135del
ENST00000676283.1:n.213_241del
ENST00000676385.2:c.-163_-135del	ENSP00000502091.1:n.-163_-135del
ENST00000676434.1:c.-163_-135del	ENSP00000501648.1:n.-163_-135del
ENST00000677389.1:c.-163_-135del MANE Plus Clinical	ENSP00000503633.1:n.-163_-135del
ENST00000347559.6:c.-163_-135del	ENSP00000292304.3:n.-163_-135del
ENST00000361308.8:c.-163_-135del	ENSP00000355292.5:n.-163_-135del
ENST00000368299.7:c.-163_-135del	ENSP00000357282.3:n.-163_-135del
ENST00000368300.8:c.-163_-135del	ENSP00000357283.4:n.-163_-135del
ENST00000368301.6:c.-163_-135del	ENSP00000357284.2:n.-163_-135del
ENST00000469565.6:n.44_72del
ENST00000470199.2:n.46_74del
ENST00000478063.2:n.46_74del
ENST00000502751.5:n.329-15861_329-15833del
ENST00000515711.1:n.487_515del
NM_001282625.1:c.-163_-135del	NP_001269554.1:n.-163_-135del
NM_001282626.1:c.-163_-135del	NP_001269555.1:n.-163_-135del
NM_005572.3:c.-163_-135del , LRG_254t1:c.-163_-135del	NP_005563.1:n.-163_-135del
NM_170707.3:c.-163_-135del	NP_733821.1:n.-163_-135del
NM_170708.3:c.-163_-135del	NP_733822.1:n.-163_-135del
XR_921781.1:n.87_115del
XR_921781.2:n.85_113del
NM_170707.4:c.-163_-135del MANE Select	NP_733821.1:n.-163_-135del
NM_001282626.2:c.-163_-135del	NP_001269555.1:n.-163_-135del
NM_001282625.2:c.-163_-135del	NP_001269554.1:n.-163_-135del
NM_005572.4:c.-163_-135del MANE Plus Clinical	NP_005563.1:n.-163_-135del
NM_170708.4:c.-163_-135del	NP_733822.1:n.-163_-135del