Canonical Allele Identifier: CA385676738
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246258A>G , CM000674.2:g.65246258A>G GRCh38
NC_000012.11:g.65640038A>G , CM000674.1:g.65640038A>G GRCh37
NC_000012.10:g.63926305A>G NCBI36
NG_016210.1:g.81688A>G
NG_016210.2:g.81688A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2669A>G MANE Select ENSP00000308369.2:p.Lys890Arg
ENST00000308330.2:c.2669A>G ENSP00000308369.2:p.Lys890Arg
ENST00000539442.1:n.651A>G
ENST00000544506.1:n.389A>G
ENST00000545026.1:n.487A>G
NM_001167614.1:c.2666A>G NP_001161086.1:p.Lys889Arg
NM_014319.4:c.2669A>G NP_055134.2:p.Lys890Arg
NM_014319.5:c.2669A>G MANE Select NP_055134.2:p.Lys890Arg
NM_001167614.2:c.2666A>G NP_001161086.1:p.Lys889Arg