Canonical Allele Identifier: CA2042456448
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246209C= , CM000674.2:g.65246209C= GRCh38
NC_000012.11:g.65639989C= , CM000674.1:g.65639989C= GRCh37
NC_000012.10:g.63926256C= NCBI36
NG_016210.1:g.81639C=
NG_016210.2:g.81639C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2620C= MANE Select ENSP00000308369.2:p.Arg874=
ENST00000308330.2:c.2620C= ENSP00000308369.2:p.Arg874=
ENST00000539442.1:n.602C=
ENST00000544506.1:n.340C=
ENST00000545026.1:n.438C=
NM_001167614.1:c.2617C= NP_001161086.1:p.Arg873=
NM_014319.4:c.2620C= NP_055134.2:p.Arg874=
NM_014319.5:c.2620C= MANE Select NP_055134.2:p.Arg874=
NM_001167614.2:c.2617C= NP_001161086.1:p.Arg873=