Canonical Allele Identifier: CA2042456608
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246273T= , CM000674.2:g.65246273T= GRCh38
NC_000012.11:g.65640053T= , CM000674.1:g.65640053T= GRCh37
NC_000012.10:g.63926320T= NCBI36
NG_016210.1:g.81703T=
NG_016210.2:g.81703T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2684T= MANE Select ENSP00000308369.2:p.Met895=
ENST00000308330.2:c.2684T= ENSP00000308369.2:p.Met895=
ENST00000539442.1:n.666T=
ENST00000544506.1:n.404T=
ENST00000545026.1:n.502T=
NM_001167614.1:c.2681T= NP_001161086.1:p.Met894=
NM_014319.4:c.2684T= NP_055134.2:p.Met895=
NM_014319.5:c.2684T= MANE Select NP_055134.2:p.Met895=
NM_001167614.2:c.2681T= NP_001161086.1:p.Met894=