Canonical Allele Identifier: CA353473399

Gene: LMOD3

Linked Data

• gnomAD v4: 3-69119328-G-T
• MyVariant Identifiers: chr3:g.69168479G>T (hg19) ; chr3:g.69119328G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69119328G>T , CM000665.2:g.69119328G>T	GRCh38
NC_000003.11:g.69168479G>T , CM000665.1:g.69168479G>T	GRCh37
NC_000003.10:g.69251169G>T	NCBI36
NG_041828.1:g.8268C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420581.7:c.1027C>A MANE Select	ENSP00000414670.3:p.Leu343Ile
ENST00000420581.6:c.1027C>A	ENSP00000414670.2:p.Leu343Ile
ENST00000475434.1:c.1027C>A	ENSP00000418645.1:p.Leu343Ile
ENST00000489031.5:c.1027C>A	ENSP00000417210.1:p.Leu343Ile
NM_001304418.1:c.1027C>A	NP_001291347.1:p.Leu343Ile
NM_198271.4:c.1027C>A	NP_938012.2:p.Leu343Ile
NM_001304418.3:c.1027C>A	NP_001291347.1:p.Leu343Ile
NM_198271.5:c.1027C>A MANE Select	NP_938012.2:p.Leu343Ile