Canonical Allele Identifier: CA2187454823

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929792_73929793delinsCA , CM000677.2:g.73929792_73929793delinsCA	GRCh38
NC_000015.9:g.74222133_74222134delinsCA , CM000677.1:g.74222133_74222134delinsCA	GRCh37
NC_000015.8:g.72009186_72009187delinsCA	NCBI36
NG_011466.1:g.8345_8346delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1102+1907_1102+1908delinsCA MANE Select	ENSP00000261921.7:n.1102+1907_1102+1908delinsCA
ENST00000261921.7:c.1102+1907_1102+1908delinsCA	ENSP00000261921.7:n.1102+1907_1102+1908delinsCA
ENST00000566011.5:c.1102+1907_1102+1908delinsCA	ENSP00000457827.1:n.1102+1907_1102+1908delinsCA
NM_005576.2:c.1102+1907_1102+1908delinsCA	NP_005567.2:n.1102+1907_1102+1908delinsCA
XM_011521555.1:c.1102+1907_1102+1908delinsCA	XP_011519857.1:n.1102+1907_1102+1908delinsCA
XR_931824.1:n.1435+1907_1435+1908delinsCA
NM_005576.3:c.1102+1907_1102+1908delinsCA	NP_005567.2:n.1102+1907_1102+1908delinsCA
XM_011521555.2:c.1102+1907_1102+1908delinsCA	XP_011519857.1:n.1102+1907_1102+1908delinsCA
XR_931824.2:n.1424+1907_1424+1908delinsCA
NM_005576.4:c.1102+1907_1102+1908delinsCA MANE Select	NP_005567.2:n.1102+1907_1102+1908delinsCA