Canonical Allele Identifier: CA2187454883

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929945_73929946delinsAG , CM000677.2:g.73929945_73929946delinsAG	GRCh38
NC_000015.9:g.74222286_74222287delinsAG , CM000677.1:g.74222286_74222287delinsAG	GRCh37
NC_000015.8:g.72009339_72009340delinsAG	NCBI36
NG_011466.1:g.8498_8499delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1102+2060_1102+2061delinsAG MANE Select	ENSP00000261921.7:n.1102+2060_1102+2061delinsAG
ENST00000261921.7:c.1102+2060_1102+2061delinsAG	ENSP00000261921.7:n.1102+2060_1102+2061delinsAG
ENST00000566011.5:c.1102+2060_1102+2061delinsAG	ENSP00000457827.1:n.1102+2060_1102+2061delinsAG
NM_005576.2:c.1102+2060_1102+2061delinsAG	NP_005567.2:n.1102+2060_1102+2061delinsAG
XM_011521555.1:c.1102+2060_1102+2061delinsAG	XP_011519857.1:n.1102+2060_1102+2061delinsAG
XR_931824.1:n.1435+2060_1435+2061delinsAG
NM_005576.3:c.1102+2060_1102+2061delinsAG	NP_005567.2:n.1102+2060_1102+2061delinsAG
XM_011521555.2:c.1102+2060_1102+2061delinsAG	XP_011519857.1:n.1102+2060_1102+2061delinsAG
XR_931824.2:n.1424+2060_1424+2061delinsAG
NM_005576.4:c.1102+2060_1102+2061delinsAG MANE Select	NP_005567.2:n.1102+2060_1102+2061delinsAG