Canonical Allele Identifier: CA385676439
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65639966T>C (hg19) chr12:g.65246186T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246186T>C , CM000674.2:g.65246186T>C GRCh38
NC_000012.11:g.65639966T>C , CM000674.1:g.65639966T>C GRCh37
NC_000012.10:g.63926233T>C NCBI36
NG_016210.1:g.81616T>C
NG_016210.2:g.81616T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2597T>C MANE Select ENSP00000308369.2:p.Leu866Ser
ENST00000308330.2:c.2597T>C ENSP00000308369.2:p.Leu866Ser
ENST00000539442.1:n.579T>C
ENST00000544506.1:n.317T>C
ENST00000545026.1:n.415T>C
NM_001167614.1:c.2594T>C NP_001161086.1:p.Leu865Ser
NM_014319.4:c.2597T>C NP_055134.2:p.Leu866Ser
NM_014319.5:c.2597T>C MANE Select NP_055134.2:p.Leu866Ser
NM_001167614.2:c.2594T>C NP_001161086.1:p.Leu865Ser
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