Canonical Allele Identifier: CA1373049373
Gene: LMOD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119499T= , CM000665.2:g.69119499T= GRCh38
NC_000003.11:g.69168650T= , CM000665.1:g.69168650T= GRCh37
NC_000003.10:g.69251340T= NCBI36
NG_041828.1:g.8097A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.856A= MANE Select ENSP00000414670.3:p.Thr286=
ENST00000420581.6:c.856A= ENSP00000414670.2:p.Thr286=
ENST00000475434.1:c.856A= ENSP00000418645.1:p.Thr286=
ENST00000489031.5:c.856A= ENSP00000417210.1:p.Thr286=
NM_001304418.1:c.856A= NP_001291347.1:p.Thr286=
NM_198271.4:c.856A= NP_938012.2:p.Thr286=
NM_001304418.3:c.856A= NP_001291347.1:p.Thr286=
NM_198271.5:c.856A= MANE Select NP_938012.2:p.Thr286=