Canonical Allele Identifier: CA2042463749
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170159C= , CM000674.2:g.65170159C= GRCh38
NC_000012.11:g.65563939C= , CM000674.1:g.65563939C= GRCh37
NC_000012.10:g.63850206C= NCBI36
NG_016210.1:g.5589C=
NG_016210.2:g.5589C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.563C= MANE Select ENSP00000308369.2:p.Ala188=
ENST00000308330.2:c.563C= ENSP00000308369.2:p.Ala188=
ENST00000541171.1:n.577C=
NM_001167614.1:c.563C= NP_001161086.1:p.Ala188=
NM_014319.4:c.563C= NP_055134.2:p.Ala188=
NM_014319.5:c.563C= MANE Select NP_055134.2:p.Ala188=
NM_001167614.2:c.563C= NP_001161086.1:p.Ala188=