Canonical Allele Identifier: CA919107554
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1565803017

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65247705del , CM000674.2:g.65247705del GRCh38
NC_000012.11:g.65641485del , CM000674.1:g.65641485del GRCh37
NC_000012.10:g.63927752del NCBI36
NG_016210.1:g.83135del
NG_016210.2:g.83135del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*1380del MANE Select ENSP00000308369.2:n.*1380del
ENST00000308330.2:c.*1380del ENSP00000308369.2:n.*1380del
NM_001167614.1:c.*1380del NP_001161086.1:n.*1380del
NM_014319.4:c.*1380del NP_055134.2:n.*1380del
NM_014319.5:c.*1380del MANE Select NP_055134.2:n.*1380del
NM_001167614.2:c.*1380del NP_001161086.1:n.*1380del