Canonical Allele Identifier: CA385676880
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65640082A>G (hg19) chr12:g.65246302A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246302A>G , CM000674.2:g.65246302A>G GRCh38
NC_000012.11:g.65640082A>G , CM000674.1:g.65640082A>G GRCh37
NC_000012.10:g.63926349A>G NCBI36
NG_016210.1:g.81732A>G
NG_016210.2:g.81732A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2713A>G MANE Select ENSP00000308369.2:p.Thr905Ala
ENST00000308330.2:c.2713A>G ENSP00000308369.2:p.Thr905Ala
ENST00000539442.1:n.695A>G
ENST00000545026.1:n.531A>G
NM_001167614.1:c.2710A>G NP_001161086.1:p.Thr904Ala
NM_014319.4:c.2713A>G NP_055134.2:p.Thr905Ala
NM_014319.5:c.2713A>G MANE Select NP_055134.2:p.Thr905Ala
NM_001167614.2:c.2710A>G NP_001161086.1:p.Thr904Ala
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