Canonical Allele Identifier: CA385670882
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238509G>A , CM000674.2:g.65238509G>A GRCh38
NC_000012.11:g.65632289G>A , CM000674.1:g.65632289G>A GRCh37
NC_000012.10:g.63918556G>A NCBI36
NG_016210.1:g.73939G>A
NG_016210.2:g.73939G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1703G>A MANE Select ENSP00000308369.2:p.Gly568Asp
ENST00000308330.2:c.1703G>A ENSP00000308369.2:p.Gly568Asp
NM_001167614.1:c.1700G>A NP_001161086.1:p.Gly567Asp
NM_014319.4:c.1703G>A NP_055134.2:p.Gly568Asp
NM_014319.5:c.1703G>A MANE Select NP_055134.2:p.Gly568Asp
NM_001167614.2:c.1700G>A NP_001161086.1:p.Gly567Asp