Canonical Allele Identifier: CA13436798
Gene: LMO1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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