Canonical Allele Identifier: CA691000263

Gene: LEMD3

Linked Data

• dbSNP Id: rs1421786041
• MyVariant Identifiers: chr12:g.65582245A>G (hg19) ; chr12:g.65188465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65188465A>G , CM000674.2:g.65188465A>G	GRCh38
NC_000012.11:g.65582245A>G , CM000674.1:g.65582245A>G	GRCh37
NC_000012.10:g.63868512A>G	NCBI36
NG_016210.1:g.23895A>G
NG_016210.2:g.23895A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.1522+17347A>G MANE Select	ENSP00000308369.2:n.1522+17347A>G
ENST00000308330.2:c.1522+17347A>G	ENSP00000308369.2:n.1522+17347A>G
ENST00000541171.1:n.836+18047A>G
NM_001167614.1:c.1522+17347A>G	NP_001161086.1:n.1522+17347A>G
NM_014319.4:c.1522+17347A>G	NP_055134.2:n.1522+17347A>G
NM_014319.5:c.1522+17347A>G MANE Select	NP_055134.2:n.1522+17347A>G
NM_001167614.2:c.1522+17347A>G	NP_001161086.1:n.1522+17347A>G