Canonical Allele Identifier: CA2042456795
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1871108159
gnomAD v4: 12-65246380-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246380G>A , CM000674.2:g.65246380G>A GRCh38
NC_000012.11:g.65640160G>A , CM000674.1:g.65640160G>A GRCh37
NC_000012.10:g.63926427G>A NCBI36
NG_016210.1:g.81810G>A
NG_016210.2:g.81810G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*55G>A MANE Select ENSP00000308369.2:n.*55G>A
ENST00000308330.2:c.*55G>A ENSP00000308369.2:n.*55G>A
ENST00000539442.1:n.773G>A
ENST00000545026.1:n.609G>A
NM_001167614.1:c.*55G>A NP_001161086.1:n.*55G>A
NM_014319.4:c.*55G>A NP_055134.2:n.*55G>A
NM_014319.5:c.*55G>A MANE Select NP_055134.2:n.*55G>A
NM_001167614.2:c.*55G>A NP_001161086.1:n.*55G>A
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