Canonical Allele Identifier: CA238907688
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs967905005

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170081G>A , CM000674.2:g.65170081G>A GRCh38
NC_000012.11:g.65563861G>A , CM000674.1:g.65563861G>A GRCh37
NC_000012.10:g.63850128G>A NCBI36
NG_016210.1:g.5511G>A
NG_016210.2:g.5511G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.485G>A MANE Select ENSP00000308369.2:p.Arg162Gln
ENST00000308330.2:c.485G>A ENSP00000308369.2:p.Arg162Gln
ENST00000541171.1:n.499G>A
NM_001167614.1:c.485G>A NP_001161086.1:p.Arg162Gln
NM_014319.4:c.485G>A NP_055134.2:p.Arg162Gln
NM_014319.5:c.485G>A MANE Select NP_055134.2:p.Arg162Gln
NM_001167614.2:c.485G>A NP_001161086.1:p.Arg162Gln