Canonical Allele Identifier: CA385673219
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170059G>C , CM000674.2:g.65170059G>C GRCh38
NC_000012.11:g.65563839G>C , CM000674.1:g.65563839G>C GRCh37
NC_000012.10:g.63850106G>C NCBI36
NG_016210.1:g.5489G>C
NG_016210.2:g.5489G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.463G>C MANE Select ENSP00000308369.2:p.Gly155Arg
ENST00000308330.2:c.463G>C ENSP00000308369.2:p.Gly155Arg
ENST00000541171.1:n.477G>C
NM_001167614.1:c.463G>C NP_001161086.1:p.Gly155Arg
NM_014319.4:c.463G>C NP_055134.2:p.Gly155Arg
NM_014319.5:c.463G>C MANE Select NP_055134.2:p.Gly155Arg
NM_001167614.2:c.463G>C NP_001161086.1:p.Gly155Arg