Canonical Allele Identifier: CA2042456166
Gene: LEMD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65245961A= , CM000674.2:g.65245961A= GRCh38
NC_000012.11:g.65639741A= , CM000674.1:g.65639741A= GRCh37
NC_000012.10:g.63926008A= NCBI36
NG_016210.1:g.81391A=
NG_016210.2:g.81391A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2572+22A= MANE Select ENSP00000308369.2:n.2572+22A=
ENST00000308330.2:c.2572+22A= ENSP00000308369.2:n.2572+22A=
ENST00000539442.1:n.554+22A=
ENST00000544506.1:n.292+22A=
ENST00000545026.1:n.390+22A=
NM_001167614.1:c.2569+22A= NP_001161086.1:n.2569+22A=
NM_014319.4:c.2572+22A= NP_055134.2:n.2572+22A=
NM_014319.5:c.2572+22A= MANE Select NP_055134.2:n.2572+22A=
NM_001167614.2:c.2569+22A= NP_001161086.1:n.2569+22A=
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