Canonical Allele Identifier: CA385673163
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170050G>T , CM000674.2:g.65170050G>T GRCh38
NC_000012.11:g.65563830G>T , CM000674.1:g.65563830G>T GRCh37
NC_000012.10:g.63850097G>T NCBI36
NG_016210.1:g.5480G>T
NG_016210.2:g.5480G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.454G>T MANE Select ENSP00000308369.2:p.Asp152Tyr
ENST00000308330.2:c.454G>T ENSP00000308369.2:p.Asp152Tyr
ENST00000541171.1:n.468G>T
NM_001167614.1:c.454G>T NP_001161086.1:p.Asp152Tyr
NM_014319.4:c.454G>T NP_055134.2:p.Asp152Tyr
NM_014319.5:c.454G>T MANE Select NP_055134.2:p.Asp152Tyr
NM_001167614.2:c.454G>T NP_001161086.1:p.Asp152Tyr