Canonical Allele Identifier: CA2187455192

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73930659C= , CM000677.2:g.73930659C=	GRCh38
NC_000015.9:g.74223000C= , CM000677.1:g.74223000C=	GRCh37
NC_000015.8:g.72010053C=	NCBI36
NG_011466.1:g.9212C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.1102+2774C= MANE Select	ENSP00000261921.7:n.1102+2774C=
ENST00000261921.7:c.1102+2774C=	ENSP00000261921.7:n.1102+2774C=
ENST00000566011.5:c.1102+2774C=	ENSP00000457827.1:n.1102+2774C=
NM_005576.2:c.1102+2774C=	NP_005567.2:n.1102+2774C=
XM_011521555.1:c.1102+2774C=	XP_011519857.1:n.1102+2774C=
XR_931824.1:n.1435+2774C=
NM_005576.3:c.1102+2774C=	NP_005567.2:n.1102+2774C=
XM_011521555.2:c.1102+2774C=	XP_011519857.1:n.1102+2774C=
XR_931824.2:n.1424+2774C=
NM_005576.4:c.1102+2774C= MANE Select	NP_005567.2:n.1102+2774C=