Canonical Allele Identifier: CA1373049332
Gene: LMOD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119407G= , CM000665.2:g.69119407G= GRCh38
NC_000003.11:g.69168558G= , CM000665.1:g.69168558G= GRCh37
NC_000003.10:g.69251248G= NCBI36
NG_041828.1:g.8189C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.948C= MANE Select ENSP00000414670.3:p.Asn316=
ENST00000420581.6:c.948C= ENSP00000414670.2:p.Asn316=
ENST00000475434.1:c.948C= ENSP00000418645.1:p.Asn316=
ENST00000489031.5:c.948C= ENSP00000417210.1:p.Asn316=
NM_001304418.1:c.948C= NP_001291347.1:p.Asn316=
NM_198271.4:c.948C= NP_938012.2:p.Asn316=
NM_001304418.3:c.948C= NP_001291347.1:p.Asn316=
NM_198271.5:c.948C= MANE Select NP_938012.2:p.Asn316=