Canonical Allele Identifier: CA2564034139
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65245999A>G , CM000674.2:g.65245999A>G GRCh38
NC_000012.11:g.65639779A>G , CM000674.1:g.65639779A>G GRCh37
NC_000012.10:g.63926046A>G NCBI36
NG_016210.1:g.81429A>G
NG_016210.2:g.81429A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2572+60A>G MANE Select ENSP00000308369.2:n.2572+60A>G
ENST00000308330.2:c.2572+60A>G ENSP00000308369.2:n.2572+60A>G
ENST00000539442.1:n.554+60A>G
ENST00000544506.1:n.292+60A>G
ENST00000545026.1:n.390+60A>G
NM_001167614.1:c.2569+60A>G NP_001161086.1:n.2569+60A>G
NM_014319.4:c.2572+60A>G NP_055134.2:n.2572+60A>G
NM_014319.5:c.2572+60A>G MANE Select NP_055134.2:n.2572+60A>G
NM_001167614.2:c.2569+60A>G NP_001161086.1:n.2569+60A>G