Canonical Allele Identifier: CA2619670986
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65247669C>A , CM000674.2:g.65247669C>A GRCh38
NC_000012.11:g.65641449C>A , CM000674.1:g.65641449C>A GRCh37
NC_000012.10:g.63927716C>A NCBI36
NG_016210.1:g.83099C>A
NG_016210.2:g.83099C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*1344C>A MANE Select ENSP00000308369.2:n.*1344C>A
ENST00000308330.2:c.*1344C>A ENSP00000308369.2:n.*1344C>A
NM_001167614.1:c.*1344C>A NP_001161086.1:n.*1344C>A
NM_014319.4:c.*1344C>A NP_055134.2:n.*1344C>A
NM_014319.5:c.*1344C>A MANE Select NP_055134.2:n.*1344C>A
NM_001167614.2:c.*1344C>A NP_001161086.1:n.*1344C>A