Canonical Allele Identifier: CA2187454944

Gene: LOXL1

Linked Data

• dbSNP Id: rs2068625387

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73930086_73930087insAGTA , CM000677.2:g.73930086_73930087insAGTA	GRCh38
NC_000015.9:g.74222427_74222428insAGTA , CM000677.1:g.74222427_74222428insAGTA	GRCh37
NC_000015.8:g.72009480_72009481insAGTA	NCBI36
NG_011466.1:g.8639_8640insAGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1102+2201_1102+2202insAGTA MANE Select	ENSP00000261921.7:n.1102+2201_1102+2202insAGTA
ENST00000261921.7:c.1102+2201_1102+2202insAGTA	ENSP00000261921.7:n.1102+2201_1102+2202insAGTA
ENST00000566011.5:c.1102+2201_1102+2202insAGTA	ENSP00000457827.1:n.1102+2201_1102+2202insAGTA
NM_005576.2:c.1102+2201_1102+2202insAGTA	NP_005567.2:n.1102+2201_1102+2202insAGTA
XM_011521555.1:c.1102+2201_1102+2202insAGTA	XP_011519857.1:n.1102+2201_1102+2202insAGTA
XR_931824.1:n.1435+2201_1435+2202insAGTA
NM_005576.3:c.1102+2201_1102+2202insAGTA	NP_005567.2:n.1102+2201_1102+2202insAGTA
XM_011521555.2:c.1102+2201_1102+2202insAGTA	XP_011519857.1:n.1102+2201_1102+2202insAGTA
XR_931824.2:n.1424+2201_1424+2202insAGTA
NM_005576.4:c.1102+2201_1102+2202insAGTA MANE Select	NP_005567.2:n.1102+2201_1102+2202insAGTA