Canonical Allele Identifier: CA385676876
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65640080T>A (hg19) chr12:g.65246300T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246300T>A , CM000674.2:g.65246300T>A GRCh38
NC_000012.11:g.65640080T>A , CM000674.1:g.65640080T>A GRCh37
NC_000012.10:g.63926347T>A NCBI36
NG_016210.1:g.81730T>A
NG_016210.2:g.81730T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2711T>A MANE Select ENSP00000308369.2:p.Leu904Gln
ENST00000308330.2:c.2711T>A ENSP00000308369.2:p.Leu904Gln
ENST00000539442.1:n.693T>A
ENST00000545026.1:n.529T>A
NM_001167614.1:c.2708T>A NP_001161086.1:p.Leu903Gln
NM_014319.4:c.2711T>A NP_055134.2:p.Leu904Gln
NM_014319.5:c.2711T>A MANE Select NP_055134.2:p.Leu904Gln
NM_001167614.2:c.2708T>A NP_001161086.1:p.Leu903Gln
Search 100 bp 5'
Search 100 bp 3'