Canonical Allele Identifier: CA2726559137
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs2136354596
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239936del , CM000674.2:g.65239936del GRCh38
NC_000012.11:g.65633716del , CM000674.1:g.65633716del GRCh37
NC_000012.10:g.63919983del NCBI36
NG_016210.1:g.75366del
NG_016210.2:g.75366del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1929del MANE Select ENSP00000308369.2:p.Met644TrpfsTer9
ENST00000308330.2:c.1929del ENSP00000308369.2:p.Met644TrpfsTer9
NM_001167614.1:c.1926del NP_001161086.1:p.Met643TrpfsTer9
NM_014319.4:c.1929del NP_055134.2:p.Met644TrpfsTer9
NM_014319.5:c.1929del MANE Select NP_055134.2:p.Met644TrpfsTer9
NM_001167614.2:c.1926del NP_001161086.1:p.Met643TrpfsTer9
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