Canonical Allele Identifier: CA342826490

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156108317C>G (hg19) ; chr1:g.156138526C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156138526C>G , CM000663.2:g.156138526C>G	GRCh38
NC_000001.10:g.156108317C>G , CM000663.1:g.156108317C>G	GRCh37
NC_000001.9:g.154374941C>G	NCBI36
NG_008692.2:g.60954C>G , LRG_254:g.60954C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.1179C>G	ENSP00000426535.3:p.Tyr393Ter
ENST00000682650.1:c.1647C>G	ENSP00000506904.1:p.Tyr549Ter
ENST00000683032.1:c.1737C>G	ENSP00000506771.1:p.Tyr579Ter
ENST00000683773.1:n.82C>G
ENST00000684195.1:c.*829C>G	ENSP00000508220.1:n.*829C>G
ENST00000361308.9:c.1737C>G	ENSP00000355292.6:p.Tyr579Ter
ENST00000368300.9:c.1737C>G MANE Select	ENSP00000357283.4:p.Tyr579Ter
ENST00000496738.6:n.2940C>G
ENST00000674518.1:c.*1087C>G	ENSP00000502261.1:n.*1087C>G
ENST00000674600.1:c.*1536C>G	ENSP00000501666.1:n.*1536C>G
ENST00000674720.1:c.*1043C>G	ENSP00000502798.1:n.*1043C>G
ENST00000675455.1:c.*1537C>G	ENSP00000501795.1:n.*1537C>G
ENST00000675667.1:c.1737C>G	ENSP00000501803.1:p.Tyr579Ter
ENST00000675874.1:c.*1208C>G	ENSP00000501851.1:n.*1208C>G
ENST00000675881.1:c.*748C>G	ENSP00000501670.1:n.*748C>G
ENST00000675939.1:c.1737C>G	ENSP00000502256.1:p.Tyr579Ter
ENST00000675989.1:n.3340C>G
ENST00000676208.1:c.*840C>G	ENSP00000502468.1:n.*840C>G
ENST00000676283.1:n.3277C>G
ENST00000676385.2:c.1647C>G	ENSP00000502091.1:p.Tyr549Ter
ENST00000676434.1:c.*1492C>G	ENSP00000501648.1:n.*1492C>G
ENST00000347559.6:c.1647C>G	ENSP00000292304.3:p.Tyr549Ter
ENST00000368299.7:c.1737C>G	ENSP00000357282.3:p.Tyr579Ter
ENST00000368300.8:c.1737C>G	ENSP00000357283.4:p.Tyr579Ter
ENST00000448611.6:c.1401C>G	ENSP00000395597.2:p.Tyr467Ter
ENST00000473598.6:c.1440C>G	ENSP00000421821.1:p.Tyr480Ter
ENST00000496738.5:n.1950C>G
ENST00000506981.1:n.321C>G
ENST00000508500.1:c.525C>G	ENSP00000424977.1:p.Tyr175Ter
NM_001257374.2:c.1401C>G	NP_001244303.1:p.Tyr467Ter
NM_001282626.1:c.1737C>G	NP_001269555.1:p.Tyr579Ter
NM_170707.3:c.1737C>G	NP_733821.1:p.Tyr579Ter
NM_170708.3:c.1647C>G	NP_733822.1:p.Tyr549Ter
XM_011509533.1:c.1401C>G	XP_011507835.1:p.Tyr467Ter
XM_011509534.1:c.1113C>G	XP_011507836.1:p.Tyr371Ter
XR_921781.1:n.2026C>G
XM_011509534.2:c.1113C>G	XP_011507836.1:p.Tyr371Ter
XR_921781.2:n.2024C>G
NM_170707.4:c.1737C>G MANE Select	NP_733821.1:p.Tyr579Ter
NM_001257374.3:c.1401C>G	NP_001244303.1:p.Tyr467Ter
NM_001282626.2:c.1737C>G	NP_001269555.1:p.Tyr579Ter
NM_170708.4:c.1647C>G	NP_733822.1:p.Tyr549Ter