Canonical Allele Identifier: CA2042463798

Gene: LEMD3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65170189G= , CM000674.2:g.65170189G=	GRCh38
NC_000012.11:g.65563969G= , CM000674.1:g.65563969G=	GRCh37
NC_000012.10:g.63850236G=	NCBI36
NG_016210.1:g.5619G=
NG_016210.2:g.5619G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.593G= MANE Select	ENSP00000308369.2:p.Gly198=
ENST00000308330.2:c.593G=	ENSP00000308369.2:p.Gly198=
ENST00000541171.1:n.607G=
NM_001167614.1:c.593G=	NP_001161086.1:p.Gly198=
NM_014319.4:c.593G=	NP_055134.2:p.Gly198=
NM_014319.5:c.593G= MANE Select	NP_055134.2:p.Gly198=
NM_001167614.2:c.593G=	NP_001161086.1:p.Gly198=