Canonical Allele Identifier: CA385673394

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65563896C>G (hg19) ; chr12:g.65170116C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65170116C>G , CM000674.2:g.65170116C>G	GRCh38
NC_000012.11:g.65563896C>G , CM000674.1:g.65563896C>G	GRCh37
NC_000012.10:g.63850163C>G	NCBI36
NG_016210.1:g.5546C>G
NG_016210.2:g.5546C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.520C>G MANE Select	ENSP00000308369.2:p.Pro174Ala
ENST00000308330.2:c.520C>G	ENSP00000308369.2:p.Pro174Ala
ENST00000541171.1:n.534C>G
NM_001167614.1:c.520C>G	NP_001161086.1:p.Pro174Ala
NM_014319.4:c.520C>G	NP_055134.2:p.Pro174Ala
NM_014319.5:c.520C>G MANE Select	NP_055134.2:p.Pro174Ala
NM_001167614.2:c.520C>G	NP_001161086.1:p.Pro174Ala