Canonical Allele Identifier: CA2042456282
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246094C= , CM000674.2:g.65246094C= GRCh38
NC_000012.11:g.65639874C= , CM000674.1:g.65639874C= GRCh37
NC_000012.10:g.63926141C= NCBI36
NG_016210.1:g.81524C=
NG_016210.2:g.81524C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2573-68C= MANE Select ENSP00000308369.2:n.2573-68C=
ENST00000308330.2:c.2573-68C= ENSP00000308369.2:n.2573-68C=
ENST00000539442.1:n.555-68C=
ENST00000544506.1:n.293-68C=
ENST00000545026.1:n.391-68C=
NM_001167614.1:c.2570-68C= NP_001161086.1:n.2570-68C=
NM_014319.4:c.2573-68C= NP_055134.2:n.2573-68C=
NM_014319.5:c.2573-68C= MANE Select NP_055134.2:n.2573-68C=
NM_001167614.2:c.2570-68C= NP_001161086.1:n.2570-68C=