Canonical Allele Identifier: CA6671087
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs757507566

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239971G>A , CM000674.2:g.65239971G>A GRCh38
NC_000012.11:g.65633751G>A , CM000674.1:g.65633751G>A GRCh37
NC_000012.10:g.63920018G>A NCBI36
NG_016210.1:g.75401G>A
NG_016210.2:g.75401G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1964G>A MANE Select ENSP00000308369.2:p.Arg655Gln
ENST00000308330.2:c.1964G>A ENSP00000308369.2:p.Arg655Gln
NM_001167614.1:c.1961G>A NP_001161086.1:p.Arg654Gln
NM_014319.4:c.1964G>A NP_055134.2:p.Arg655Gln
NM_014319.5:c.1964G>A MANE Select NP_055134.2:p.Arg655Gln
NM_001167614.2:c.1961G>A NP_001161086.1:p.Arg654Gln