Canonical Allele Identifier: CA2042463795

Gene: LEMD3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65170187G= , CM000674.2:g.65170187G=	GRCh38
NC_000012.11:g.65563967G= , CM000674.1:g.65563967G=	GRCh37
NC_000012.10:g.63850234G=	NCBI36
NG_016210.1:g.5617G=
NG_016210.2:g.5617G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.591G= MANE Select	ENSP00000308369.2:p.Trp197=
ENST00000308330.2:c.591G=	ENSP00000308369.2:p.Trp197=
ENST00000541171.1:n.605G=
NM_001167614.1:c.591G=	NP_001161086.1:p.Trp197=
NM_014319.4:c.591G=	NP_055134.2:p.Trp197=
NM_014319.5:c.591G= MANE Select	NP_055134.2:p.Trp197=
NM_001167614.2:c.591G=	NP_001161086.1:p.Trp197=