Canonical Allele Identifier: CA1951029613
Gene: LMO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8231306A= , CM000673.2:g.8231306A= GRCh38
NC_000011.9:g.8252853A= , CM000673.1:g.8252853A= GRCh37
NC_000011.8:g.8209429A= NCBI36
NG_032827.2:g.42330T=
NG_032827.3:g.42330T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335790.8:c.26-802T= MANE Select ENSP00000338207.3:n.26-802T=
ENST00000335790.7:c.26-802T= ENSP00000338207.3:n.26-802T=
ENST00000428101.6:c.23-802T= ENSP00000404538.2:n.23-802T=
ENST00000524379.1:n.52-802T=
ENST00000534484.1:c.-8-802T= ENSP00000435456.1:n.-8-802T=
NM_001270428.1:c.23-802T= NP_001257357.1:n.23-802T=
NM_002315.2:c.26-802T= NP_002306.1:n.26-802T=
NR_073006.1:n.542-802T=
XM_006718228.2:c.137-802T= XP_006718291.1:n.137-802T=
XM_011520096.1:c.113-802T= XP_011518398.1:n.113-802T=
XM_011520097.1:c.26-802T= XP_011518399.1:n.26-802T=
XM_011520098.1:c.-8-802T= XP_011518400.1:n.-8-802T=
XM_011520099.1:c.-8-802T= XP_011518401.1:n.-8-802T=
XR_931013.1:n.555+222A=
XR_931014.1:n.555+222A=
XM_006718228.3:c.137-802T= XP_006718291.1:n.137-802T=
XM_011520098.2:c.-8-802T= XP_011518400.1:n.-8-802T=
XM_011520099.2:c.-8-802T= XP_011518401.1:n.-8-802T=
XR_001748117.1:n.779A=
XR_931013.2:n.557+222A=
XR_931014.2:n.557+222A=
NM_002315.3:c.26-802T= MANE Select NP_002306.1:n.26-802T=
NM_001270428.2:c.23-802T= NP_001257357.1:n.23-802T=
NR_073006.2:n.542-802T=