Canonical Allele Identifier: CA1728654

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74533609G>C , CM000664.2:g.74533609G>C	GRCh38
NC_000002.11:g.74760736G>C , CM000664.1:g.74760736G>C	GRCh37
NC_000002.10:g.74614244G>C	NCBI36
NG_012163.1:g.9205G>C
NG_033037.1:g.1239C>G
NG_033047.1:g.25327C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.2259C>G MANE Select	ENSP00000264094.3:p.Ile753Met
ENST00000264094.7:c.2259C>G	ENSP00000264094.3:p.Ile753Met
ENST00000393937.6:c.1824C>G	ENSP00000377512.2:p.Ile608Met
ENST00000409249.5:c.1413C>G	ENSP00000387103.1:p.Ile471Met
ENST00000409549.5:c.2091C>G	ENSP00000386696.1:p.Ile697Met
ENST00000470907.6:n.1642C>G
NM_001289164.1:c.1824C>G	NP_001276093.1:p.Ile608Met
NM_001289165.1:c.1176C>G	NP_001276094.1:p.Ile392Met
NM_032603.3:c.2259C>G	NP_115992.1:p.Ile753Met
XM_011533134.1:c.2259C>G	XP_011531436.1:p.Ile753Met
NM_001289164.2:c.1824C>G	NP_001276093.1:p.Ile608Met
NM_032603.4:c.2259C>G	NP_115992.1:p.Ile753Met
XM_011533134.2:c.2259C>G	XP_011531436.1:p.Ile753Met
XM_017005112.1:c.1176C>G	XP_016860601.1:p.Ile392Met
XM_024453176.1:c.2259C>G	XP_024308944.1:p.Ile753Met
XM_024453177.1:c.2259C>G	XP_024308945.1:p.Ile753Met
XM_024453178.1:c.2259C>G	XP_024308946.1:p.Ile753Met
NM_032603.5:c.2259C>G MANE Select	NP_115992.1:p.Ile753Met
NM_001289164.3:c.1824C>G	NP_001276093.1:p.Ile608Met
NM_001289165.2:c.1176C>G	NP_001276094.1:p.Ile392Met