Canonical Allele Identifier: CA2042456202
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65245984G= , CM000674.2:g.65245984G= GRCh38
NC_000012.11:g.65639764G= , CM000674.1:g.65639764G= GRCh37
NC_000012.10:g.63926031G= NCBI36
NG_016210.1:g.81414G=
NG_016210.2:g.81414G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2572+45G= MANE Select ENSP00000308369.2:n.2572+45G=
ENST00000308330.2:c.2572+45G= ENSP00000308369.2:n.2572+45G=
ENST00000539442.1:n.554+45G=
ENST00000544506.1:n.292+45G=
ENST00000545026.1:n.390+45G=
NM_001167614.1:c.2569+45G= NP_001161086.1:n.2569+45G=
NM_014319.4:c.2572+45G= NP_055134.2:n.2572+45G=
NM_014319.5:c.2572+45G= MANE Select NP_055134.2:n.2572+45G=
NM_001167614.2:c.2569+45G= NP_001161086.1:n.2569+45G=