Canonical Allele Identifier: CA2042456307
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246115A= , CM000674.2:g.65246115A= GRCh38
NC_000012.11:g.65639895A= , CM000674.1:g.65639895A= GRCh37
NC_000012.10:g.63926162A= NCBI36
NG_016210.1:g.81545A=
NG_016210.2:g.81545A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2573-47A= MANE Select ENSP00000308369.2:n.2573-47A=
ENST00000308330.2:c.2573-47A= ENSP00000308369.2:n.2573-47A=
ENST00000539442.1:n.555-47A=
ENST00000544506.1:n.293-47A=
ENST00000545026.1:n.391-47A=
NM_001167614.1:c.2570-47A= NP_001161086.1:n.2570-47A=
NM_014319.4:c.2573-47A= NP_055134.2:n.2573-47A=
NM_014319.5:c.2573-47A= MANE Select NP_055134.2:n.2573-47A=
NM_001167614.2:c.2570-47A= NP_001161086.1:n.2570-47A=