Canonical Allele Identifier: CA347384522

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74534225G>A , CM000664.2:g.74534225G>A	GRCh38
NC_000002.11:g.74761352G>A , CM000664.1:g.74761352G>A	GRCh37
NC_000002.10:g.74614860G>A	NCBI36
NG_012163.1:g.9821G>A
NG_033037.1:g.623C>T
NG_033047.1:g.24711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.1951C>T MANE Select	ENSP00000264094.3:p.Arg651Trp
ENST00000264094.7:c.1951C>T	ENSP00000264094.3:p.Arg651Trp
ENST00000393937.6:c.1516C>T	ENSP00000377512.2:p.Arg506Trp
ENST00000409249.5:c.1105C>T	ENSP00000387103.1:p.Arg369Trp
ENST00000409549.5:c.1783C>T	ENSP00000386696.1:p.Arg595Trp
ENST00000409986.5:c.1516C>T	ENSP00000386545.1:p.Arg506Trp
ENST00000470907.6:n.1334C>T
NM_001289164.1:c.1516C>T	NP_001276093.1:p.Arg506Trp
NM_001289165.1:c.868C>T	NP_001276094.1:p.Arg290Trp
NM_032603.3:c.1951C>T	NP_115992.1:p.Arg651Trp
XM_011533134.1:c.1951C>T	XP_011531436.1:p.Arg651Trp
NM_001289164.2:c.1516C>T	NP_001276093.1:p.Arg506Trp
NM_032603.4:c.1951C>T	NP_115992.1:p.Arg651Trp
XM_011533134.2:c.1951C>T	XP_011531436.1:p.Arg651Trp
XM_017005112.1:c.868C>T	XP_016860601.1:p.Arg290Trp
XM_024453176.1:c.1951C>T	XP_024308944.1:p.Arg651Trp
XM_024453177.1:c.1951C>T	XP_024308945.1:p.Arg651Trp
XM_024453178.1:c.1951C>T	XP_024308946.1:p.Arg651Trp
NM_032603.5:c.1951C>T MANE Select	NP_115992.1:p.Arg651Trp
NM_001289164.3:c.1516C>T	NP_001276093.1:p.Arg506Trp
NM_001289165.2:c.868C>T	NP_001276094.1:p.Arg290Trp