Canonical Allele Identifier: CA50490700

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74534224C>T , CM000664.2:g.74534224C>T	GRCh38
NC_000002.11:g.74761351C>T , CM000664.1:g.74761351C>T	GRCh37
NC_000002.10:g.74614859C>T	NCBI36
NG_012163.1:g.9820C>T
NG_033037.1:g.624G>A
NG_033047.1:g.24712G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.1952G>A MANE Select	ENSP00000264094.3:p.Arg651Gln
ENST00000264094.7:c.1952G>A	ENSP00000264094.3:p.Arg651Gln
ENST00000393937.6:c.1517G>A	ENSP00000377512.2:p.Arg506Gln
ENST00000409249.5:c.1106G>A	ENSP00000387103.1:p.Arg369Gln
ENST00000409549.5:c.1784G>A	ENSP00000386696.1:p.Arg595Gln
ENST00000409986.5:c.1517G>A	ENSP00000386545.1:p.Arg506Gln
ENST00000470907.6:n.1335G>A
NM_001289164.1:c.1517G>A	NP_001276093.1:p.Arg506Gln
NM_001289165.1:c.869G>A	NP_001276094.1:p.Arg290Gln
NM_032603.3:c.1952G>A	NP_115992.1:p.Arg651Gln
XM_011533134.1:c.1952G>A	XP_011531436.1:p.Arg651Gln
NM_001289164.2:c.1517G>A	NP_001276093.1:p.Arg506Gln
NM_032603.4:c.1952G>A	NP_115992.1:p.Arg651Gln
XM_011533134.2:c.1952G>A	XP_011531436.1:p.Arg651Gln
XM_017005112.1:c.869G>A	XP_016860601.1:p.Arg290Gln
XM_024453176.1:c.1952G>A	XP_024308944.1:p.Arg651Gln
XM_024453177.1:c.1952G>A	XP_024308945.1:p.Arg651Gln
XM_024453178.1:c.1952G>A	XP_024308946.1:p.Arg651Gln
NM_032603.5:c.1952G>A MANE Select	NP_115992.1:p.Arg651Gln
NM_001289164.3:c.1517G>A	NP_001276093.1:p.Arg506Gln
NM_001289165.2:c.869G>A	NP_001276094.1:p.Arg290Gln