Canonical Allele Identifier: CA13436802
Gene: LMO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8242978T>C , CM000673.2:g.8242978T>C GRCh38
NC_000011.9:g.8264525T>C , CM000673.1:g.8264525T>C GRCh37
NC_000011.8:g.8221101T>C NCBI36
NG_032827.2:g.30658A>G
NG_032827.3:g.30658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000335790.8:c.26-12474A>G MANE Select ENSP00000338207.3:n.26-12474A>G
ENST00000335790.7:c.26-12474A>G ENSP00000338207.3:n.26-12474A>G
ENST00000428101.6:c.23-12474A>G ENSP00000404538.2:n.23-12474A>G
ENST00000524379.1:n.52-12474A>G
ENST00000534484.1:c.-8-12474A>G ENSP00000435456.1:n.-8-12474A>G
NM_001270428.1:c.23-12474A>G NP_001257357.1:n.23-12474A>G
NM_002315.2:c.26-12474A>G NP_002306.1:n.26-12474A>G
NR_073006.1:n.542-12474A>G
XM_011520097.1:c.26-12474A>G XP_011518399.1:n.26-12474A>G
XM_011520099.1:c.-8-12474A>G XP_011518401.1:n.-8-12474A>G
XM_011520099.2:c.-8-12474A>G XP_011518401.1:n.-8-12474A>G
NM_002315.3:c.26-12474A>G MANE Select NP_002306.1:n.26-12474A>G
NM_001270428.2:c.23-12474A>G NP_001257357.1:n.23-12474A>G
NR_073006.2:n.542-12474A>G