Canonical Allele Identifier: CA655113398
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65247625_65247626insG , CM000674.2:g.65247625_65247626insG GRCh38
NC_000012.11:g.65641405_65641406insG , CM000674.1:g.65641405_65641406insG GRCh37
NC_000012.10:g.63927672_63927673insG NCBI36
NG_016210.1:g.83055_83056insG
NG_016210.2:g.83055_83056insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*1300_*1301insG MANE Select ENSP00000308369.2:n.*1300_*1301insG
ENST00000308330.2:c.*1300_*1301insG ENSP00000308369.2:n.*1300_*1301insG
NM_001167614.1:c.*1300_*1301insG NP_001161086.1:n.*1300_*1301insG
NM_014319.4:c.*1300_*1301insG NP_055134.2:n.*1300_*1301insG
NM_014319.5:c.*1300_*1301insG MANE Select NP_055134.2:n.*1300_*1301insG
NM_001167614.2:c.*1300_*1301insG NP_001161086.1:n.*1300_*1301insG