Canonical Allele Identifier: CA385676697
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246248C>G , CM000674.2:g.65246248C>G GRCh38
NC_000012.11:g.65640028C>G , CM000674.1:g.65640028C>G GRCh37
NC_000012.10:g.63926295C>G NCBI36
NG_016210.1:g.81678C>G
NG_016210.2:g.81678C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2659C>G MANE Select ENSP00000308369.2:p.Pro887Ala
ENST00000308330.2:c.2659C>G ENSP00000308369.2:p.Pro887Ala
ENST00000539442.1:n.641C>G
ENST00000544506.1:n.379C>G
ENST00000545026.1:n.477C>G
NM_001167614.1:c.2656C>G NP_001161086.1:p.Pro886Ala
NM_014319.4:c.2659C>G NP_055134.2:p.Pro887Ala
NM_014319.5:c.2659C>G MANE Select NP_055134.2:p.Pro887Ala
NM_001167614.2:c.2656C>G NP_001161086.1:p.Pro886Ala