Canonical Allele Identifier: CA385672880
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65563762C>G (hg19) chr12:g.65169982C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65169982C>G , CM000674.2:g.65169982C>G GRCh38
NC_000012.11:g.65563762C>G , CM000674.1:g.65563762C>G GRCh37
NC_000012.10:g.63850029C>G NCBI36
NG_016210.1:g.5412C>G
NG_016210.2:g.5412C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.386C>G MANE Select ENSP00000308369.2:p.Pro129Arg
ENST00000308330.2:c.386C>G ENSP00000308369.2:p.Pro129Arg
ENST00000541171.1:n.400C>G
NM_001167614.1:c.386C>G NP_001161086.1:p.Pro129Arg
NM_014319.4:c.386C>G NP_055134.2:p.Pro129Arg
NM_014319.5:c.386C>G MANE Select NP_055134.2:p.Pro129Arg
NM_001167614.2:c.386C>G NP_001161086.1:p.Pro129Arg
Search 100 bp 5'
Search 100 bp 3'