Canonical Allele Identifier: CA2619670580
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246053del , CM000674.2:g.65246053del GRCh38
NC_000012.11:g.65639833del , CM000674.1:g.65639833del GRCh37
NC_000012.10:g.63926100del NCBI36
NG_016210.1:g.81483del
NG_016210.2:g.81483del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2573-109del MANE Select ENSP00000308369.2:n.2573-109del
ENST00000308330.2:c.2573-109del ENSP00000308369.2:n.2573-109del
ENST00000539442.1:n.555-109del
ENST00000544506.1:n.293-109del
ENST00000545026.1:n.391-109del
NM_001167614.1:c.2570-109del NP_001161086.1:n.2570-109del
NM_014319.4:c.2573-109del NP_055134.2:n.2573-109del
NM_014319.5:c.2573-109del MANE Select NP_055134.2:n.2573-109del
NM_001167614.2:c.2570-109del NP_001161086.1:n.2570-109del