Canonical Allele Identifier: CA2042444001

Gene: LEMD3

Linked Data

• dbSNP Id: rs1592462017

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65238355dup , CM000674.2:g.65238355dup	GRCh38
NC_000012.11:g.65632135dup , CM000674.1:g.65632135dup	GRCh37
NC_000012.10:g.63918402dup	NCBI36
NG_016210.1:g.73785dup
NG_016210.2:g.73785dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.1696-147dup MANE Select	ENSP00000308369.2:n.1696-147dup
ENST00000308330.2:c.1696-147dup	ENSP00000308369.2:n.1696-147dup
NM_001167614.1:c.1693-147dup	NP_001161086.1:n.1693-147dup
NM_014319.4:c.1696-147dup	NP_055134.2:n.1696-147dup
NM_014319.5:c.1696-147dup MANE Select	NP_055134.2:n.1696-147dup
NM_001167614.2:c.1693-147dup	NP_001161086.1:n.1693-147dup