Canonical Allele Identifier: CA1373049239
Gene: LMOD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119304T= , CM000665.2:g.69119304T= GRCh38
NC_000003.11:g.69168455T= , CM000665.1:g.69168455T= GRCh37
NC_000003.10:g.69251145T= NCBI36
NG_041828.1:g.8292A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.1051A= MANE Select ENSP00000414670.3:p.Met351=
ENST00000420581.6:c.1051A= ENSP00000414670.2:p.Met351=
ENST00000475434.1:c.1051A= ENSP00000418645.1:p.Met351=
ENST00000489031.5:c.1051A= ENSP00000417210.1:p.Met351=
NM_001304418.1:c.1051A= NP_001291347.1:p.Met351=
NM_198271.4:c.1051A= NP_938012.2:p.Met351=
NM_001304418.3:c.1051A= NP_001291347.1:p.Met351=
NM_198271.5:c.1051A= MANE Select NP_938012.2:p.Met351=