Canonical Allele Identifier: CA2042444002
Gene: LEMD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238350T= , CM000674.2:g.65238350T= GRCh38
NC_000012.11:g.65632130T= , CM000674.1:g.65632130T= GRCh37
NC_000012.10:g.63918397T= NCBI36
NG_016210.1:g.73780T=
NG_016210.2:g.73780T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-152T= MANE Select ENSP00000308369.2:n.1696-152T=
ENST00000308330.2:c.1696-152T= ENSP00000308369.2:n.1696-152T=
NM_001167614.1:c.1693-152T= NP_001161086.1:n.1693-152T=
NM_014319.4:c.1696-152T= NP_055134.2:n.1696-152T=
NM_014319.5:c.1696-152T= MANE Select NP_055134.2:n.1696-152T=
NM_001167614.2:c.1693-152T= NP_001161086.1:n.1693-152T=
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