Canonical Allele Identifier: CA2187454857

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929884_73929885delinsTG , CM000677.2:g.73929884_73929885delinsTG	GRCh38
NC_000015.9:g.74222225_74222226delinsTG , CM000677.1:g.74222225_74222226delinsTG	GRCh37
NC_000015.8:g.72009278_72009279delinsTG	NCBI36
NG_011466.1:g.8437_8438delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1102+1999_1102+2000delinsTG MANE Select	ENSP00000261921.7:n.1102+1999_1102+2000delinsTG
ENST00000261921.7:c.1102+1999_1102+2000delinsTG	ENSP00000261921.7:n.1102+1999_1102+2000delinsTG
ENST00000566011.5:c.1102+1999_1102+2000delinsTG	ENSP00000457827.1:n.1102+1999_1102+2000delinsTG
NM_005576.2:c.1102+1999_1102+2000delinsTG	NP_005567.2:n.1102+1999_1102+2000delinsTG
XM_011521555.1:c.1102+1999_1102+2000delinsTG	XP_011519857.1:n.1102+1999_1102+2000delinsTG
XR_931824.1:n.1435+1999_1435+2000delinsTG
NM_005576.3:c.1102+1999_1102+2000delinsTG	NP_005567.2:n.1102+1999_1102+2000delinsTG
XM_011521555.2:c.1102+1999_1102+2000delinsTG	XP_011519857.1:n.1102+1999_1102+2000delinsTG
XR_931824.2:n.1424+1999_1424+2000delinsTG
NM_005576.4:c.1102+1999_1102+2000delinsTG MANE Select	NP_005567.2:n.1102+1999_1102+2000delinsTG