Canonical Allele Identifier: CA2042444659
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238774T= , CM000674.2:g.65238774T= GRCh38
NC_000012.11:g.65632554T= , CM000674.1:g.65632554T= GRCh37
NC_000012.10:g.63918821T= NCBI36
NG_016210.1:g.74204T=
NG_016210.2:g.74204T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1881T= MANE Select ENSP00000308369.2:p.Ala627=
ENST00000308330.2:c.1881T= ENSP00000308369.2:p.Ala627=
NM_001167614.1:c.1878T= NP_001161086.1:p.Ala626=
NM_014319.4:c.1881T= NP_055134.2:p.Ala627=
NM_014319.5:c.1881T= MANE Select NP_055134.2:p.Ala627=
NM_001167614.2:c.1878T= NP_001161086.1:p.Ala626=