Canonical Allele Identifier: CA2042443990

Gene: LEMD3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65238339_65238342delinsCTTT , CM000674.2:g.65238339_65238342delinsCTTT	GRCh38
NC_000012.11:g.65632119_65632122delinsCTTT , CM000674.1:g.65632119_65632122delinsCTTT	GRCh37
NC_000012.10:g.63918386_63918389delinsCTTT	NCBI36
NG_016210.1:g.73769_73772delinsCTTT
NG_016210.2:g.73769_73772delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.1696-163_1696-160delinsCTTT MANE Select	ENSP00000308369.2:n.1696-163_1696-160delinsCTTT
ENST00000308330.2:c.1696-163_1696-160delinsCTTT	ENSP00000308369.2:n.1696-163_1696-160delinsCTTT
NM_001167614.1:c.1693-163_1693-160delinsCTTT	NP_001161086.1:n.1693-163_1693-160delinsCTTT
NM_014319.4:c.1696-163_1696-160delinsCTTT	NP_055134.2:n.1696-163_1696-160delinsCTTT
NM_014319.5:c.1696-163_1696-160delinsCTTT MANE Select	NP_055134.2:n.1696-163_1696-160delinsCTTT
NM_001167614.2:c.1693-163_1693-160delinsCTTT	NP_001161086.1:n.1693-163_1693-160delinsCTTT