Canonical Allele Identifier: CA2619669381
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238395_65238398del , CM000674.2:g.65238395_65238398del GRCh38
NC_000012.11:g.65632175_65632178del , CM000674.1:g.65632175_65632178del GRCh37
NC_000012.10:g.63918442_63918445del NCBI36
NG_016210.1:g.73825_73828del
NG_016210.2:g.73825_73828del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-107_1696-104del MANE Select ENSP00000308369.2:n.1696-107_1696-104del
ENST00000308330.2:c.1696-107_1696-104del ENSP00000308369.2:n.1696-107_1696-104del
NM_001167614.1:c.1693-107_1693-104del NP_001161086.1:n.1693-107_1693-104del
NM_014319.4:c.1696-107_1696-104del NP_055134.2:n.1696-107_1696-104del
NM_014319.5:c.1696-107_1696-104del MANE Select NP_055134.2:n.1696-107_1696-104del
NM_001167614.2:c.1693-107_1693-104del NP_001161086.1:n.1693-107_1693-104del