Canonical Allele Identifier: CA2619670564
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246018del , CM000674.2:g.65246018del GRCh38
NC_000012.11:g.65639798del , CM000674.1:g.65639798del GRCh37
NC_000012.10:g.63926065del NCBI36
NG_016210.1:g.81448del
NG_016210.2:g.81448del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2572+79del MANE Select ENSP00000308369.2:n.2572+79del
ENST00000308330.2:c.2572+79del ENSP00000308369.2:n.2572+79del
ENST00000539442.1:n.554+79del
ENST00000544506.1:n.292+79del
ENST00000545026.1:n.390+79del
NM_001167614.1:c.2569+79del NP_001161086.1:n.2569+79del
NM_014319.4:c.2572+79del NP_055134.2:n.2572+79del
NM_014319.5:c.2572+79del MANE Select NP_055134.2:n.2572+79del
NM_001167614.2:c.2569+79del NP_001161086.1:n.2569+79del