Canonical Allele Identifier: CA1728807

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74534563C>A , CM000664.2:g.74534563C>A	GRCh38
NC_000002.11:g.74761690C>A , CM000664.1:g.74761690C>A	GRCh37
NC_000002.10:g.74615198C>A	NCBI36
NG_012163.1:g.10159C>A
NG_033037.1:g.285G>T
NG_033047.1:g.24373G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.1791G>T MANE Select	ENSP00000264094.3:p.Gly597=
ENST00000264094.7:c.1791G>T	ENSP00000264094.3:p.Gly597=
ENST00000393937.6:c.1356G>T	ENSP00000377512.2:p.Gly452=
ENST00000409249.5:c.1094-327G>T	ENSP00000387103.1:n.1094-327G>T
ENST00000409549.5:c.1623G>T	ENSP00000386696.1:p.Gly541=
ENST00000409986.5:c.1356G>T	ENSP00000386545.1:p.Gly452=
ENST00000470907.6:n.1174G>T
NM_001289164.1:c.1356G>T	NP_001276093.1:p.Gly452=
NM_001289165.1:c.708G>T	NP_001276094.1:p.Gly236=
NM_032603.3:c.1791G>T	NP_115992.1:p.Gly597=
XM_011533134.1:c.1791G>T	XP_011531436.1:p.Gly597=
NM_001289164.2:c.1356G>T	NP_001276093.1:p.Gly452=
NM_032603.4:c.1791G>T	NP_115992.1:p.Gly597=
XM_011533134.2:c.1791G>T	XP_011531436.1:p.Gly597=
XM_017005112.1:c.708G>T	XP_016860601.1:p.Gly236=
XM_024453176.1:c.1791G>T	XP_024308944.1:p.Gly597=
XM_024453177.1:c.1791G>T	XP_024308945.1:p.Gly597=
XM_024453178.1:c.1791G>T	XP_024308946.1:p.Gly597=
NM_032603.5:c.1791G>T MANE Select	NP_115992.1:p.Gly597=
NM_001289164.3:c.1356G>T	NP_001276093.1:p.Gly452=
NM_001289165.2:c.708G>T	NP_001276094.1:p.Gly236=