Canonical Allele Identifier: CA1728759
Gene: LOXL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74534326C>T , CM000664.2:g.74534326C>T GRCh38
NC_000002.11:g.74761453C>T , CM000664.1:g.74761453C>T GRCh37
NC_000002.10:g.74614961C>T NCBI36
NG_012163.1:g.9922C>T
NG_033037.1:g.522G>A
NG_033047.1:g.24610G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264094.8:c.1929G>A MANE Select ENSP00000264094.3:p.Glu643=
ENST00000264094.7:c.1929G>A ENSP00000264094.3:p.Glu643=
ENST00000393937.6:c.1494G>A ENSP00000377512.2:p.Glu498=
ENST00000409249.5:c.1094-90G>A ENSP00000387103.1:n.1094-90G>A
ENST00000409549.5:c.1761G>A ENSP00000386696.1:p.Glu587=
ENST00000409986.5:c.1494G>A ENSP00000386545.1:p.Glu498=
ENST00000470907.6:n.1312G>A
NM_001289164.1:c.1494G>A NP_001276093.1:p.Glu498=
NM_001289165.1:c.846G>A NP_001276094.1:p.Glu282=
NM_032603.3:c.1929G>A NP_115992.1:p.Glu643=
XM_011533134.1:c.1929G>A XP_011531436.1:p.Glu643=
NM_001289164.2:c.1494G>A NP_001276093.1:p.Glu498=
NM_032603.4:c.1929G>A NP_115992.1:p.Glu643=
XM_011533134.2:c.1929G>A XP_011531436.1:p.Glu643=
XM_017005112.1:c.846G>A XP_016860601.1:p.Glu282=
XM_024453176.1:c.1929G>A XP_024308944.1:p.Glu643=
XM_024453177.1:c.1929G>A XP_024308945.1:p.Glu643=
XM_024453178.1:c.1929G>A XP_024308946.1:p.Glu643=
NM_032603.5:c.1929G>A MANE Select NP_115992.1:p.Glu643=
NM_001289164.3:c.1494G>A NP_001276093.1:p.Glu498=
NM_001289165.2:c.846G>A NP_001276094.1:p.Glu282=