Canonical Allele Identifier: CA385676383
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246174C>A , CM000674.2:g.65246174C>A GRCh38
NC_000012.11:g.65639954C>A , CM000674.1:g.65639954C>A GRCh37
NC_000012.10:g.63926221C>A NCBI36
NG_016210.1:g.81604C>A
NG_016210.2:g.81604C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2585C>A MANE Select ENSP00000308369.2:p.Thr862Lys
ENST00000308330.2:c.2585C>A ENSP00000308369.2:p.Thr862Lys
ENST00000539442.1:n.567C>A
ENST00000544506.1:n.305C>A
ENST00000545026.1:n.403C>A
NM_001167614.1:c.2582C>A NP_001161086.1:p.Thr861Lys
NM_014319.4:c.2585C>A NP_055134.2:p.Thr862Lys
NM_014319.5:c.2585C>A MANE Select NP_055134.2:p.Thr862Lys
NM_001167614.2:c.2582C>A NP_001161086.1:p.Thr861Lys