Canonical Allele Identifier: CA2042444131
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238457G= , CM000674.2:g.65238457G= GRCh38
NC_000012.11:g.65632237G= , CM000674.1:g.65632237G= GRCh37
NC_000012.10:g.63918504G= NCBI36
NG_016210.1:g.73887G=
NG_016210.2:g.73887G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-45G= MANE Select ENSP00000308369.2:n.1696-45G=
ENST00000308330.2:c.1696-45G= ENSP00000308369.2:n.1696-45G=
NM_001167614.1:c.1693-45G= NP_001161086.1:n.1693-45G=
NM_014319.4:c.1696-45G= NP_055134.2:n.1696-45G=
NM_014319.5:c.1696-45G= MANE Select NP_055134.2:n.1696-45G=
NM_001167614.2:c.1693-45G= NP_001161086.1:n.1693-45G=