Canonical Allele Identifier: CA6671082
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs369133002

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239940G>A , CM000674.2:g.65239940G>A GRCh38
NC_000012.11:g.65633720G>A , CM000674.1:g.65633720G>A GRCh37
NC_000012.10:g.63919987G>A NCBI36
NG_016210.1:g.75370G>A
NG_016210.2:g.75370G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1933G>A MANE Select ENSP00000308369.2:p.Val645Ile
ENST00000308330.2:c.1933G>A ENSP00000308369.2:p.Val645Ile
NM_001167614.1:c.1930G>A NP_001161086.1:p.Val644Ile
NM_014319.4:c.1933G>A NP_055134.2:p.Val645Ile
NM_014319.5:c.1933G>A MANE Select NP_055134.2:p.Val645Ile
NM_001167614.2:c.1930G>A NP_001161086.1:p.Val644Ile