Canonical Allele Identifier: CA2619670647

Gene: LEMD3

Linked Data

• gnomAD v4: 12-65246374-C-CTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65246375_65246376insATT , CM000674.2:g.65246375_65246376insATT	GRCh38
NC_000012.11:g.65640155_65640156insATT , CM000674.1:g.65640155_65640156insATT	GRCh37
NC_000012.10:g.63926422_63926423insATT	NCBI36
NG_016210.1:g.81805_81806insATT
NG_016210.2:g.81805_81806insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.*50_*51insATT MANE Select	ENSP00000308369.2:n.*50_*51insATT
ENST00000308330.2:c.*50_*51insATT	ENSP00000308369.2:n.*50_*51insATT
ENST00000539442.1:n.768_769insATT
ENST00000545026.1:n.604_605insATT
NM_001167614.1:c.*50_*51insATT	NP_001161086.1:n.*50_*51insATT
NM_014319.4:c.*50_*51insATT	NP_055134.2:n.*50_*51insATT
NM_014319.5:c.*50_*51insATT MANE Select	NP_055134.2:n.*50_*51insATT
NM_001167614.2:c.*50_*51insATT	NP_001161086.1:n.*50_*51insATT