Canonical Allele Identifier: CA2042456442
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246206C= , CM000674.2:g.65246206C= GRCh38
NC_000012.11:g.65639986C= , CM000674.1:g.65639986C= GRCh37
NC_000012.10:g.63926253C= NCBI36
NG_016210.1:g.81636C=
NG_016210.2:g.81636C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2617C= MANE Select ENSP00000308369.2:p.His873=
ENST00000308330.2:c.2617C= ENSP00000308369.2:p.His873=
ENST00000539442.1:n.599C=
ENST00000544506.1:n.337C=
ENST00000545026.1:n.435C=
NM_001167614.1:c.2614C= NP_001161086.1:p.His872=
NM_014319.4:c.2617C= NP_055134.2:p.His873=
NM_014319.5:c.2617C= MANE Select NP_055134.2:p.His873=
NM_001167614.2:c.2614C= NP_001161086.1:p.His872=