Canonical Allele Identifier: CA2619669547
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239857_65239858insG , CM000674.2:g.65239857_65239858insG GRCh38
NC_000012.11:g.65633637_65633638insG , CM000674.1:g.65633637_65633638insG GRCh37
NC_000012.10:g.63919904_63919905insG NCBI36
NG_016210.1:g.75287_75288insG
NG_016210.2:g.75287_75288insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1922-72_1922-71insG MANE Select ENSP00000308369.2:n.1922-72_1922-71insG
ENST00000308330.2:c.1922-72_1922-71insG ENSP00000308369.2:n.1922-72_1922-71insG
NM_001167614.1:c.1919-72_1919-71insG NP_001161086.1:n.1919-72_1919-71insG
NM_014319.4:c.1922-72_1922-71insG NP_055134.2:n.1922-72_1922-71insG
NM_014319.5:c.1922-72_1922-71insG MANE Select NP_055134.2:n.1922-72_1922-71insG
NM_001167614.2:c.1919-72_1919-71insG NP_001161086.1:n.1919-72_1919-71insG