Canonical Allele Identifier: CA50490289

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74533647A>G , CM000664.2:g.74533647A>G	GRCh38
NC_000002.11:g.74760774A>G , CM000664.1:g.74760774A>G	GRCh37
NC_000002.10:g.74614282A>G	NCBI36
NG_012163.1:g.9243A>G
NG_033037.1:g.1201T>C
NG_033047.1:g.25289T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.2221T>C MANE Select	ENSP00000264094.3:p.Phe741Leu
ENST00000264094.7:c.2221T>C	ENSP00000264094.3:p.Phe741Leu
ENST00000393937.6:c.1786T>C	ENSP00000377512.2:p.Phe596Leu
ENST00000409249.5:c.1375T>C	ENSP00000387103.1:p.Phe459Leu
ENST00000409549.5:c.2053T>C	ENSP00000386696.1:p.Phe685Leu
ENST00000470907.6:n.1604T>C
NM_001289164.1:c.1786T>C	NP_001276093.1:p.Phe596Leu
NM_001289165.1:c.1138T>C	NP_001276094.1:p.Phe380Leu
NM_032603.3:c.2221T>C	NP_115992.1:p.Phe741Leu
XM_011533134.1:c.2221T>C	XP_011531436.1:p.Phe741Leu
NM_001289164.2:c.1786T>C	NP_001276093.1:p.Phe596Leu
NM_032603.4:c.2221T>C	NP_115992.1:p.Phe741Leu
XM_011533134.2:c.2221T>C	XP_011531436.1:p.Phe741Leu
XM_017005112.1:c.1138T>C	XP_016860601.1:p.Phe380Leu
XM_024453176.1:c.2221T>C	XP_024308944.1:p.Phe741Leu
XM_024453177.1:c.2221T>C	XP_024308945.1:p.Phe741Leu
XM_024453178.1:c.2221T>C	XP_024308946.1:p.Phe741Leu
NM_032603.5:c.2221T>C MANE Select	NP_115992.1:p.Phe741Leu
NM_001289164.3:c.1786T>C	NP_001276093.1:p.Phe596Leu
NM_001289165.2:c.1138T>C	NP_001276094.1:p.Phe380Leu