Canonical Allele Identifier: CA2042449555
Gene: LEMD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65188416C= , CM000674.2:g.65188416C= GRCh38
NC_000012.11:g.65582196C= , CM000674.1:g.65582196C= GRCh37
NC_000012.10:g.63868463C= NCBI36
NG_016210.1:g.23846C=
NG_016210.2:g.23846C=

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1522+17298C= MANE Select ENSP00000308369.2:n.1522+17298C=
ENST00000308330.2:c.1522+17298C= ENSP00000308369.2:n.1522+17298C=
ENST00000541171.1:n.836+17998C=
NM_001167614.1:c.1522+17298C= NP_001161086.1:n.1522+17298C=
NM_014319.4:c.1522+17298C= NP_055134.2:n.1522+17298C=
NM_014319.5:c.1522+17298C= MANE Select NP_055134.2:n.1522+17298C=
NM_001167614.2:c.1522+17298C= NP_001161086.1:n.1522+17298C=
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