Canonical Allele Identifier: CA385676780
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246266A>T , CM000674.2:g.65246266A>T GRCh38
NC_000012.11:g.65640046A>T , CM000674.1:g.65640046A>T GRCh37
NC_000012.10:g.63926313A>T NCBI36
NG_016210.1:g.81696A>T
NG_016210.2:g.81696A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2677A>T MANE Select ENSP00000308369.2:p.Asn893Tyr
ENST00000308330.2:c.2677A>T ENSP00000308369.2:p.Asn893Tyr
ENST00000539442.1:n.659A>T
ENST00000544506.1:n.397A>T
ENST00000545026.1:n.495A>T
NM_001167614.1:c.2674A>T NP_001161086.1:p.Asn892Tyr
NM_014319.4:c.2677A>T NP_055134.2:p.Asn893Tyr
NM_014319.5:c.2677A>T MANE Select NP_055134.2:p.Asn893Tyr
NM_001167614.2:c.2674A>T NP_001161086.1:p.Asn892Tyr