Canonical Allele Identifier: CA2187454889

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929958_73929959delinsAT , CM000677.2:g.73929958_73929959delinsAT	GRCh38
NC_000015.9:g.74222299_74222300delinsAT , CM000677.1:g.74222299_74222300delinsAT	GRCh37
NC_000015.8:g.72009352_72009353delinsAT	NCBI36
NG_011466.1:g.8511_8512delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.1102+2073_1102+2074delinsAT MANE Select	ENSP00000261921.7:n.1102+2073_1102+2074de...
ENST00000261921.7:c.1102+2073_1102+2074delinsAT	ENSP00000261921.7:n.1102+2073_1102+2074de...
ENST00000566011.5:c.1102+2073_1102+2074delinsAT	ENSP00000457827.1:n.1102+2073_1102+2074de...
NM_005576.2:c.1102+2073_1102+2074delinsAT	NP_005567.2:n.1102+2073_1102+2074delinsAT...
XM_011521555.1:c.1102+2073_1102+2074delinsAT	XP_011519857.1:n.1102+2073_1102+2074delin...
XR_931824.1:n.1435+2073_1435+2074delinsAT
NM_005576.3:c.1102+2073_1102+2074delinsAT	NP_005567.2:n.1102+2073_1102+2074delinsAT...
XM_011521555.2:c.1102+2073_1102+2074delinsAT	XP_011519857.1:n.1102+2073_1102+2074delin...
XR_931824.2:n.1424+2073_1424+2074delinsAT
NM_005576.4:c.1102+2073_1102+2074delinsAT MANE Select	NP_005567.2:n.1102+2073_1102+2074delinsAT...