Canonical Allele Identifier: CA2042458503
Gene: LEMD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65247663A= , CM000674.2:g.65247663A= GRCh38
NC_000012.11:g.65641443A= , CM000674.1:g.65641443A= GRCh37
NC_000012.10:g.63927710A= NCBI36
NG_016210.1:g.83093A=
NG_016210.2:g.83093A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*1338A= MANE Select ENSP00000308369.2:n.*1338A=
ENST00000308330.2:c.*1338A= ENSP00000308369.2:n.*1338A=
NM_001167614.1:c.*1338A= NP_001161086.1:n.*1338A=
NM_014319.4:c.*1338A= NP_055134.2:n.*1338A=
NM_014319.5:c.*1338A= MANE Select NP_055134.2:n.*1338A=
NM_001167614.2:c.*1338A= NP_001161086.1:n.*1338A=
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