Canonical Allele Identifier: CA353474119
Gene: LMOD3 HGNC NCBI

Linked Data

gnomAD v4: 3-69119460-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119460C>G , CM000665.2:g.69119460C>G GRCh38
NC_000003.11:g.69168611C>G , CM000665.1:g.69168611C>G GRCh37
NC_000003.10:g.69251301C>G NCBI36
NG_041828.1:g.8136G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.895G>C MANE Select ENSP00000414670.3:p.Ala299Pro
ENST00000420581.6:c.895G>C ENSP00000414670.2:p.Ala299Pro
ENST00000475434.1:c.895G>C ENSP00000418645.1:p.Ala299Pro
ENST00000489031.5:c.895G>C ENSP00000417210.1:p.Ala299Pro
NM_001304418.1:c.895G>C NP_001291347.1:p.Ala299Pro
NM_198271.4:c.895G>C NP_938012.2:p.Ala299Pro
NM_001304418.3:c.895G>C NP_001291347.1:p.Ala299Pro
NM_198271.5:c.895G>C MANE Select NP_938012.2:p.Ala299Pro