Canonical Allele Identifier: CA2102851005
Gene: LMO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.75674967G= , CM000675.2:g.75674967G= GRCh38
NC_000013.10:g.76249103G= , CM000675.1:g.76249103G= GRCh37
NC_000013.9:g.75147104G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377534.8:c.70-38215G= MANE Select ENSP00000366757.4:n.70-38215G=
ENST00000341547.8:c.226-38215G= ENSP00000342112.4:n.226-38215G=
ENST00000357063.7:c.181-38215G= ENSP00000349571.4:n.181-38215G=
ENST00000377499.9:c.70-38215G= ENSP00000366719.5:n.70-38215G=
ENST00000377534.7:c.70-38215G= ENSP00000366757.4:n.70-38215G=
ENST00000533305.5:n.82-38215G=
NM_001306080.1:c.70-38215G= NP_001293009.1:n.70-38215G=
NM_005358.5:c.226-38215G= NP_005349.3:n.226-38215G=
XM_017020574.2:c.-630-38215G= XP_016876063.1:n.-630-38215G=
NM_001306080.2:c.70-38215G= MANE Select NP_001293009.1:n.70-38215G=