Canonical Allele Identifier: CA480669537

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65640051C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65246271C>G , CM000674.2:g.65246271C>G	GRCh38
NC_000012.11:g.65640051C>G , CM000674.1:g.65640051C>G	GRCh37
NC_000012.10:g.63926318C>G	NCBI36
NG_016210.1:g.81701C>G
NG_016210.2:g.81701C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.2682C>G MANE Select	ENSP00000308369.2:p.Ser894=
ENST00000308330.2:c.2682C>G	ENSP00000308369.2:p.Ser894=
ENST00000539442.1:n.664C>G
ENST00000544506.1:n.402C>G
ENST00000545026.1:n.500C>G
NM_001167614.1:c.2679C>G	NP_001161086.1:p.Ser893=
NM_014319.4:c.2682C>G	NP_055134.2:p.Ser894=
NM_014319.5:c.2682C>G MANE Select	NP_055134.2:p.Ser894=
NM_001167614.2:c.2679C>G	NP_001161086.1:p.Ser893=