Canonical Allele Identifier: CA353473312

Gene: LMOD3

Linked Data

• MyVariant Identifiers: chr3:g.69168461T>A (hg19) ; chr3:g.69119310T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69119310T>A , CM000665.2:g.69119310T>A	GRCh38
NC_000003.11:g.69168461T>A , CM000665.1:g.69168461T>A	GRCh37
NC_000003.10:g.69251151T>A	NCBI36
NG_041828.1:g.8286A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420581.7:c.1045A>T MANE Select	ENSP00000414670.3:p.Arg349Trp
ENST00000420581.6:c.1045A>T	ENSP00000414670.2:p.Arg349Trp
ENST00000475434.1:c.1045A>T	ENSP00000418645.1:p.Arg349Trp
ENST00000489031.5:c.1045A>T	ENSP00000417210.1:p.Arg349Trp
NM_001304418.1:c.1045A>T	NP_001291347.1:p.Arg349Trp
NM_198271.4:c.1045A>T	NP_938012.2:p.Arg349Trp
NM_001304418.3:c.1045A>T	NP_001291347.1:p.Arg349Trp
NM_198271.5:c.1045A>T MANE Select	NP_938012.2:p.Arg349Trp