Canonical Allele Identifier: CA2726559090
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs2136360081
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65247657G>A , CM000674.2:g.65247657G>A GRCh38
NC_000012.11:g.65641437G>A , CM000674.1:g.65641437G>A GRCh37
NC_000012.10:g.63927704G>A NCBI36
NG_016210.1:g.83087G>A
NG_016210.2:g.83087G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*1332G>A MANE Select ENSP00000308369.2:n.*1332G>A
ENST00000308330.2:c.*1332G>A ENSP00000308369.2:n.*1332G>A
NM_001167614.1:c.*1332G>A NP_001161086.1:n.*1332G>A
NM_014319.4:c.*1332G>A NP_055134.2:n.*1332G>A
NM_014319.5:c.*1332G>A MANE Select NP_055134.2:n.*1332G>A
NM_001167614.2:c.*1332G>A NP_001161086.1:n.*1332G>A
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