Canonical Allele Identifier: CA1728718

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74534089A>T , CM000664.2:g.74534089A>T	GRCh38
NC_000002.11:g.74761216A>T , CM000664.1:g.74761216A>T	GRCh37
NC_000002.10:g.74614724A>T	NCBI36
NG_012163.1:g.9685A>T
NG_033037.1:g.759T>A
NG_033047.1:g.24847T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032603.5:c.2076+11T>A MANE Select	NP_115992.1:n.2076+11T>A
ENST00000264094.8:c.2076+11T>A MANE Select	ENSP00000264094.3:n.2076+11T>A
NM_001289164.1:c.1641+11T>A	NP_001276093.1:n.1641+11T>A
NM_001289164.2:c.1641+11T>A	NP_001276093.1:n.1641+11T>A
NM_001289164.3:c.1641+11T>A	NP_001276093.1:n.1641+11T>A
NM_001289165.1:c.993+11T>A	NP_001276094.1:n.993+11T>A
NM_001289165.2:c.993+11T>A	NP_001276094.1:n.993+11T>A
NM_032603.3:c.2076+11T>A	NP_115992.1:n.2076+11T>A
NM_032603.4:c.2076+11T>A	NP_115992.1:n.2076+11T>A
ENST00000264094.7:c.2076+11T>A	ENSP00000264094.3:n.2076+11T>A
ENST00000393937.6:c.1641+11T>A	ENSP00000377512.2:n.1641+11T>A
ENST00000409249.5:c.1230+11T>A	ENSP00000387103.1:n.1230+11T>A
ENST00000409549.5:c.1908+11T>A	ENSP00000386696.1:n.1908+11T>A
ENST00000409986.5:c.1641+11T>A	ENSP00000386545.1:n.1641+11T>A
ENST00000470907.6:n.1459+11T>A
XM_011533134.1:c.2076+11T>A	XP_011531436.1:n.2076+11T>A
XM_011533134.2:c.2076+11T>A	XP_011531436.1:n.2076+11T>A
XM_017005112.1:c.993+11T>A	XP_016860601.1:n.993+11T>A
XM_024453176.1:c.2076+11T>A	XP_024308944.1:n.2076+11T>A
XM_024453177.1:c.2076+11T>A	XP_024308945.1:n.2076+11T>A
XM_024453178.1:c.2076+11T>A	XP_024308946.1:n.2076+11T>A