Canonical Allele Identifier: CA480669800

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65640090T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65246310T>A , CM000674.2:g.65246310T>A	GRCh38
NC_000012.11:g.65640090T>A , CM000674.1:g.65640090T>A	GRCh37
NC_000012.10:g.63926357T>A	NCBI36
NG_016210.1:g.81740T>A
NG_016210.2:g.81740T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.2721T>A MANE Select	ENSP00000308369.2:p.Ser907=
ENST00000308330.2:c.2721T>A	ENSP00000308369.2:p.Ser907=
ENST00000539442.1:n.703T>A
ENST00000545026.1:n.539T>A
NM_001167614.1:c.2718T>A	NP_001161086.1:p.Ser906=
NM_014319.4:c.2721T>A	NP_055134.2:p.Ser907=
NM_014319.5:c.2721T>A MANE Select	NP_055134.2:p.Ser907=
NM_001167614.2:c.2718T>A	NP_001161086.1:p.Ser906=