Canonical Allele Identifier: CA2042443997

Gene: LEMD3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65238349_65238350delinsCT , CM000674.2:g.65238349_65238350delinsCT	GRCh38
NC_000012.11:g.65632129_65632130delinsCT , CM000674.1:g.65632129_65632130delinsCT	GRCh37
NC_000012.10:g.63918396_63918397delinsCT	NCBI36
NG_016210.1:g.73779_73780delinsCT
NG_016210.2:g.73779_73780delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.1696-153_1696-152delinsCT MANE Select	ENSP00000308369.2:n.1696-153_1696-152delinsCT
ENST00000308330.2:c.1696-153_1696-152delinsCT	ENSP00000308369.2:n.1696-153_1696-152delinsCT
NM_001167614.1:c.1693-153_1693-152delinsCT	NP_001161086.1:n.1693-153_1693-152delinsCT
NM_014319.4:c.1696-153_1696-152delinsCT	NP_055134.2:n.1696-153_1696-152delinsCT
NM_014319.5:c.1696-153_1696-152delinsCT MANE Select	NP_055134.2:n.1696-153_1696-152delinsCT
NM_001167614.2:c.1693-153_1693-152delinsCT	NP_001161086.1:n.1693-153_1693-152delinsCT