Canonical Allele Identifier: CA480668816

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65639943G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65246163G>T , CM000674.2:g.65246163G>T	GRCh38
NC_000012.11:g.65639943G>T , CM000674.1:g.65639943G>T	GRCh37
NC_000012.10:g.63926210G>T	NCBI36
NG_016210.1:g.81593G>T
NG_016210.2:g.81593G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.2574G>T MANE Select	ENSP00000308369.2:p.Gly858=
ENST00000308330.2:c.2574G>T	ENSP00000308369.2:p.Gly858=
ENST00000539442.1:n.556G>T
ENST00000544506.1:n.294G>T
ENST00000545026.1:n.392G>T
NM_001167614.1:c.2571G>T	NP_001161086.1:p.Gly857=
NM_014319.4:c.2574G>T	NP_055134.2:p.Gly858=
NM_014319.5:c.2574G>T MANE Select	NP_055134.2:p.Gly858=
NM_001167614.2:c.2571G>T	NP_001161086.1:p.Gly857=