Canonical Allele Identifier: CA2042463754
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170163G= , CM000674.2:g.65170163G= GRCh38
NC_000012.11:g.65563943G= , CM000674.1:g.65563943G= GRCh37
NC_000012.10:g.63850210G= NCBI36
NG_016210.1:g.5593G=
NG_016210.2:g.5593G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.567G= MANE Select ENSP00000308369.2:p.Glu189=
ENST00000308330.2:c.567G= ENSP00000308369.2:p.Glu189=
ENST00000541171.1:n.581G=
NM_001167614.1:c.567G= NP_001161086.1:p.Glu189=
NM_014319.4:c.567G= NP_055134.2:p.Glu189=
NM_014319.5:c.567G= MANE Select NP_055134.2:p.Glu189=
NM_001167614.2:c.567G= NP_001161086.1:p.Glu189=