Canonical Allele Identifier: CA347384297

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74534126C>T , CM000664.2:g.74534126C>T	GRCh38
NC_000002.11:g.74761253C>T , CM000664.1:g.74761253C>T	GRCh37
NC_000002.10:g.74614761C>T	NCBI36
NG_012163.1:g.9722C>T
NG_033037.1:g.722G>A
NG_033047.1:g.24810G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.2050G>A MANE Select	ENSP00000264094.3:p.Val684Met
ENST00000264094.7:c.2050G>A	ENSP00000264094.3:p.Val684Met
ENST00000393937.6:c.1615G>A	ENSP00000377512.2:p.Val539Met
ENST00000409249.5:c.1204G>A	ENSP00000387103.1:p.Val402Met
ENST00000409549.5:c.1882G>A	ENSP00000386696.1:p.Val628Met
ENST00000409986.5:c.1615G>A	ENSP00000386545.1:p.Val539Met
ENST00000470907.6:n.1433G>A
NM_001289164.1:c.1615G>A	NP_001276093.1:p.Val539Met
NM_001289165.1:c.967G>A	NP_001276094.1:p.Val323Met
NM_032603.3:c.2050G>A	NP_115992.1:p.Val684Met
XM_011533134.1:c.2050G>A	XP_011531436.1:p.Val684Met
NM_001289164.2:c.1615G>A	NP_001276093.1:p.Val539Met
NM_032603.4:c.2050G>A	NP_115992.1:p.Val684Met
XM_011533134.2:c.2050G>A	XP_011531436.1:p.Val684Met
XM_017005112.1:c.967G>A	XP_016860601.1:p.Val323Met
XM_024453176.1:c.2050G>A	XP_024308944.1:p.Val684Met
XM_024453177.1:c.2050G>A	XP_024308945.1:p.Val684Met
XM_024453178.1:c.2050G>A	XP_024308946.1:p.Val684Met
NM_032603.5:c.2050G>A MANE Select	NP_115992.1:p.Val684Met
NM_001289164.3:c.1615G>A	NP_001276093.1:p.Val539Met
NM_001289165.2:c.967G>A	NP_001276094.1:p.Val323Met