Canonical Allele Identifier: CA385671198
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238733A>T , CM000674.2:g.65238733A>T GRCh38
NC_000012.11:g.65632513A>T , CM000674.1:g.65632513A>T GRCh37
NC_000012.10:g.63918780A>T NCBI36
NG_016210.1:g.74163A>T
NG_016210.2:g.74163A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1840A>T MANE Select ENSP00000308369.2:p.Thr614Ser
ENST00000308330.2:c.1840A>T ENSP00000308369.2:p.Thr614Ser
NM_001167614.1:c.1837A>T NP_001161086.1:p.Thr613Ser
NM_014319.4:c.1840A>T NP_055134.2:p.Thr614Ser
NM_014319.5:c.1840A>T MANE Select NP_055134.2:p.Thr614Ser
NM_001167614.2:c.1837A>T NP_001161086.1:p.Thr613Ser