Canonical Allele Identifier: CA2042443960
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238307_65238308delinsCT , CM000674.2:g.65238307_65238308delinsCT GRCh38
NC_000012.11:g.65632087_65632088delinsCT , CM000674.1:g.65632087_65632088delinsCT GRCh37
NC_000012.10:g.63918354_63918355delinsCT NCBI36
NG_016210.1:g.73737_73738delinsCT
NG_016210.2:g.73737_73738delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-195_1696-194delinsCT MANE Select ENSP00000308369.2:n.1696-195_1696-194delinsCT
ENST00000308330.2:c.1696-195_1696-194delinsCT ENSP00000308369.2:n.1696-195_1696-194delinsCT
NM_001167614.1:c.1693-195_1693-194delinsCT NP_001161086.1:n.1693-195_1693-194delinsCT
NM_014319.4:c.1696-195_1696-194delinsCT NP_055134.2:n.1696-195_1696-194delinsCT
NM_014319.5:c.1696-195_1696-194delinsCT MANE Select NP_055134.2:n.1696-195_1696-194delinsCT
NM_001167614.2:c.1693-195_1693-194delinsCT NP_001161086.1:n.1693-195_1693-194delinsCT