Canonical Allele Identifier: CA427039877

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74534428A>G , CM000664.2:g.74534428A>G	GRCh38
NC_000002.11:g.74761555A>G , CM000664.1:g.74761555A>G	GRCh37
NC_000002.10:g.74615063A>G	NCBI36
NG_012163.1:g.10024A>G
NG_033037.1:g.420T>C
NG_033047.1:g.24508T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.1827T>C MANE Select	ENSP00000264094.3:p.His609=
ENST00000264094.7:c.1827T>C	ENSP00000264094.3:p.His609=
ENST00000393937.6:c.1392T>C	ENSP00000377512.2:p.His464=
ENST00000409249.5:c.1094-192T>C	ENSP00000387103.1:n.1094-192T>C
ENST00000409549.5:c.1659T>C	ENSP00000386696.1:p.His553=
ENST00000409986.5:c.1392T>C	ENSP00000386545.1:p.His464=
ENST00000470907.6:n.1210T>C
NM_001289164.1:c.1392T>C	NP_001276093.1:p.His464=
NM_001289165.1:c.744T>C	NP_001276094.1:p.His248=
NM_032603.3:c.1827T>C	NP_115992.1:p.His609=
XM_011533134.1:c.1827T>C	XP_011531436.1:p.His609=
NM_001289164.2:c.1392T>C	NP_001276093.1:p.His464=
NM_032603.4:c.1827T>C	NP_115992.1:p.His609=
XM_011533134.2:c.1827T>C	XP_011531436.1:p.His609=
XM_017005112.1:c.744T>C	XP_016860601.1:p.His248=
XM_024453176.1:c.1827T>C	XP_024308944.1:p.His609=
XM_024453177.1:c.1827T>C	XP_024308945.1:p.His609=
XM_024453178.1:c.1827T>C	XP_024308946.1:p.His609=
NM_032603.5:c.1827T>C MANE Select	NP_115992.1:p.His609=
NM_001289164.3:c.1392T>C	NP_001276093.1:p.His464=
NM_001289165.2:c.744T>C	NP_001276094.1:p.His248=