Canonical Allele Identifier: CA480669436

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65640036T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65246256T>C , CM000674.2:g.65246256T>C	GRCh38
NC_000012.11:g.65640036T>C , CM000674.1:g.65640036T>C	GRCh37
NC_000012.10:g.63926303T>C	NCBI36
NG_016210.1:g.81686T>C
NG_016210.2:g.81686T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.2667T>C MANE Select	ENSP00000308369.2:p.Asn889=
ENST00000308330.2:c.2667T>C	ENSP00000308369.2:p.Asn889=
ENST00000539442.1:n.649T>C
ENST00000544506.1:n.387T>C
ENST00000545026.1:n.485T>C
NM_001167614.1:c.2664T>C	NP_001161086.1:p.Asn888=
NM_014319.4:c.2667T>C	NP_055134.2:p.Asn889=
NM_014319.5:c.2667T>C MANE Select	NP_055134.2:p.Asn889=
NM_001167614.2:c.2664T>C	NP_001161086.1:p.Asn888=