Canonical Allele Identifier: CA2619670559
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246006A>T , CM000674.2:g.65246006A>T GRCh38
NC_000012.11:g.65639786A>T , CM000674.1:g.65639786A>T GRCh37
NC_000012.10:g.63926053A>T NCBI36
NG_016210.1:g.81436A>T
NG_016210.2:g.81436A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2572+67A>T MANE Select ENSP00000308369.2:n.2572+67A>T
ENST00000308330.2:c.2572+67A>T ENSP00000308369.2:n.2572+67A>T
ENST00000539442.1:n.554+67A>T
ENST00000544506.1:n.292+67A>T
ENST00000545026.1:n.390+67A>T
NM_001167614.1:c.2569+67A>T NP_001161086.1:n.2569+67A>T
NM_014319.4:c.2572+67A>T NP_055134.2:n.2572+67A>T
NM_014319.5:c.2572+67A>T MANE Select NP_055134.2:n.2572+67A>T
NM_001167614.2:c.2569+67A>T NP_001161086.1:n.2569+67A>T