Canonical Allele Identifier: CA1261472673

Gene: LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74534552_74534554del , CM000664.2:g.74534552_74534554del	GRCh38
NC_000002.11:g.74761679_74761681del , CM000664.1:g.74761679_74761681del	GRCh37
NC_000002.10:g.74615187_74615189del	NCBI36
NG_012163.1:g.10148_10150del
NG_033037.1:g.294_296del
NG_033047.1:g.24382_24384del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264094.8:c.1800_1802del MANE Select	ENSP00000264094.3:p.Trp601del
ENST00000264094.7:c.1800_1802del	ENSP00000264094.3:p.Trp601del
ENST00000393937.6:c.1365_1367del	ENSP00000377512.2:p.Trp456del
ENST00000409249.5:c.1094-318_1094-316del	ENSP00000387103.1:n.1094-318_1094-316del
ENST00000409549.5:c.1632_1634del	ENSP00000386696.1:p.Trp545del
ENST00000409986.5:c.1365_1367del	ENSP00000386545.1:p.Trp456del
ENST00000470907.6:n.1183_1185del
NM_001289164.1:c.1365_1367del	NP_001276093.1:p.Trp456del
NM_001289165.1:c.717_719del	NP_001276094.1:p.Trp240del
NM_032603.3:c.1800_1802del	NP_115992.1:p.Trp601del
XM_011533134.1:c.1800_1802del	XP_011531436.1:p.Trp601del
NM_001289164.2:c.1365_1367del	NP_001276093.1:p.Trp456del
NM_032603.4:c.1800_1802del	NP_115992.1:p.Trp601del
XM_011533134.2:c.1800_1802del	XP_011531436.1:p.Trp601del
XM_017005112.1:c.717_719del	XP_016860601.1:p.Trp240del
XM_024453176.1:c.1800_1802del	XP_024308944.1:p.Trp601del
XM_024453177.1:c.1800_1802del	XP_024308945.1:p.Trp601del
XM_024453178.1:c.1800_1802del	XP_024308946.1:p.Trp601del
NM_032603.5:c.1800_1802del MANE Select	NP_115992.1:p.Trp601del
NM_001289164.3:c.1365_1367del	NP_001276093.1:p.Trp456del
NM_001289165.2:c.717_719del	NP_001276094.1:p.Trp240del