Canonical Allele Identifier: CA385676752
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246261A>T , CM000674.2:g.65246261A>T GRCh38
NC_000012.11:g.65640041A>T , CM000674.1:g.65640041A>T GRCh37
NC_000012.10:g.63926308A>T NCBI36
NG_016210.1:g.81691A>T
NG_016210.2:g.81691A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2672A>T MANE Select ENSP00000308369.2:p.His891Leu
ENST00000308330.2:c.2672A>T ENSP00000308369.2:p.His891Leu
ENST00000539442.1:n.654A>T
ENST00000544506.1:n.392A>T
ENST00000545026.1:n.490A>T
NM_001167614.1:c.2669A>T NP_001161086.1:p.His890Leu
NM_014319.4:c.2672A>T NP_055134.2:p.His891Leu
NM_014319.5:c.2672A>T MANE Select NP_055134.2:p.His891Leu
NM_001167614.2:c.2669A>T NP_001161086.1:p.His890Leu