Canonical Allele Identifier: CA2187454874

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929933_73929937delinsTGTTA , CM000677.2:g.73929933_73929937delinsTGTTA	GRCh38
NC_000015.9:g.74222274_74222278delinsTGTTA , CM000677.1:g.74222274_74222278delinsTGTTA	GRCh37
NC_000015.8:g.72009327_72009331delinsTGTTA	NCBI36
NG_011466.1:g.8486_8490delinsTGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1102+2048_1102+2052delinsTGTTA MANE Select	ENSP00000261921.7:n.1102+2048_1102+2052delinsTGTTA
ENST00000261921.7:c.1102+2048_1102+2052delinsTGTTA	ENSP00000261921.7:n.1102+2048_1102+2052delinsTGTTA
ENST00000566011.5:c.1102+2048_1102+2052delinsTGTTA	ENSP00000457827.1:n.1102+2048_1102+2052delinsTGTTA
NM_005576.2:c.1102+2048_1102+2052delinsTGTTA	NP_005567.2:n.1102+2048_1102+2052delinsTGTTA
XM_011521555.1:c.1102+2048_1102+2052delinsTGTTA	XP_011519857.1:n.1102+2048_1102+2052delinsTGTTA
XR_931824.1:n.1435+2048_1435+2052delinsTGTTA
NM_005576.3:c.1102+2048_1102+2052delinsTGTTA	NP_005567.2:n.1102+2048_1102+2052delinsTGTTA
XM_011521555.2:c.1102+2048_1102+2052delinsTGTTA	XP_011519857.1:n.1102+2048_1102+2052delinsTGTTA
XR_931824.2:n.1424+2048_1424+2052delinsTGTTA
NM_005576.4:c.1102+2048_1102+2052delinsTGTTA MANE Select	NP_005567.2:n.1102+2048_1102+2052delinsTGTTA