Canonical Allele Identifier: CA2042456242
Gene: LEMD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246060C= , CM000674.2:g.65246060C= GRCh38
NC_000012.11:g.65639840C= , CM000674.1:g.65639840C= GRCh37
NC_000012.10:g.63926107C= NCBI36
NG_016210.1:g.81490C=
NG_016210.2:g.81490C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2573-102C= MANE Select ENSP00000308369.2:n.2573-102C=
ENST00000308330.2:c.2573-102C= ENSP00000308369.2:n.2573-102C=
ENST00000539442.1:n.555-102C=
ENST00000544506.1:n.293-102C=
ENST00000545026.1:n.391-102C=
NM_001167614.1:c.2570-102C= NP_001161086.1:n.2570-102C=
NM_014319.4:c.2573-102C= NP_055134.2:n.2573-102C=
NM_014319.5:c.2573-102C= MANE Select NP_055134.2:n.2573-102C=
NM_001167614.2:c.2570-102C= NP_001161086.1:n.2570-102C=
Search 100 bp 5'
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