Canonical Allele Identifier: CA2619670669
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246416T>A , CM000674.2:g.65246416T>A GRCh38
NC_000012.11:g.65640196T>A , CM000674.1:g.65640196T>A GRCh37
NC_000012.10:g.63926463T>A NCBI36
NG_016210.1:g.81846T>A
NG_016210.2:g.81846T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*91T>A MANE Select ENSP00000308369.2:n.*91T>A
ENST00000308330.2:c.*91T>A ENSP00000308369.2:n.*91T>A
ENST00000539442.1:n.809T>A
NM_001167614.1:c.*91T>A NP_001161086.1:n.*91T>A
NM_014319.4:c.*91T>A NP_055134.2:n.*91T>A
NM_014319.5:c.*91T>A MANE Select NP_055134.2:n.*91T>A
NM_001167614.2:c.*91T>A NP_001161086.1:n.*91T>A