Canonical Allele Identifier: CA385673532
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65563962T>G (hg19) chr12:g.65170182T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170182T>G , CM000674.2:g.65170182T>G GRCh38
NC_000012.11:g.65563962T>G , CM000674.1:g.65563962T>G GRCh37
NC_000012.10:g.63850229T>G NCBI36
NG_016210.1:g.5612T>G
NG_016210.2:g.5612T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.586T>G MANE Select ENSP00000308369.2:p.Trp196Gly
ENST00000308330.2:c.586T>G ENSP00000308369.2:p.Trp196Gly
ENST00000541171.1:n.600T>G
NM_001167614.1:c.586T>G NP_001161086.1:p.Trp196Gly
NM_014319.4:c.586T>G NP_055134.2:p.Trp196Gly
NM_014319.5:c.586T>G MANE Select NP_055134.2:p.Trp196Gly
NM_001167614.2:c.586T>G NP_001161086.1:p.Trp196Gly
Search 100 bp 5'
Search 100 bp 3'