Canonical Allele Identifier: CA2042446722
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65240052_65240056delinsCAACT , CM000674.2:g.65240052_65240056delinsCAACT GRCh38
NC_000012.11:g.65633832_65633836delinsCAACT , CM000674.1:g.65633832_65633836delinsCAACT GRCh37
NC_000012.10:g.63920099_63920103delinsCAACT NCBI36
NG_016210.1:g.75482_75486delinsCAACT
NG_016210.2:g.75482_75486delinsCAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2023+22_2023+26delinsCAACT MANE Select ENSP00000308369.2:n.2023+22_2023+26delinsCAACT
ENST00000308330.2:c.2023+22_2023+26delinsCAACT ENSP00000308369.2:n.2023+22_2023+26delinsCAACT
NM_001167614.1:c.2020+22_2020+26delinsCAACT NP_001161086.1:n.2020+22_2020+26delinsCAACT
NM_014319.4:c.2023+22_2023+26delinsCAACT NP_055134.2:n.2023+22_2023+26delinsCAACT
NM_014319.5:c.2023+22_2023+26delinsCAACT MANE Select NP_055134.2:n.2023+22_2023+26delinsCAACT
NM_001167614.2:c.2020+22_2020+26delinsCAACT NP_001161086.1:n.2020+22_2020+26delinsCAACT