Canonical Allele Identifier: CA2187466148

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73949178_73949180delinsCCT , CM000677.2:g.73949178_73949180delinsCCT	GRCh38
NC_000015.9:g.74241519_74241521delinsCCT , CM000677.1:g.74241519_74241521delinsCCT	GRCh37
NC_000015.8:g.72028572_72028574delinsCCT	NCBI36
NG_011466.1:g.27731_27733delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1603-281_1603-279delinsCCT MANE Select	ENSP00000261921.7:n.1603-281_1603-279delinsCCT
ENST00000261921.7:c.1603-281_1603-279delinsCCT	ENSP00000261921.7:n.1603-281_1603-279delinsCCT
ENST00000562548.1:n.688-281_688-279delinsCCT
ENST00000566011.5:c.*491-281_*491-279delinsCCT	ENSP00000457827.1:n.*491-281_*491-279delinsCCT
ENST00000566530.1:n.441-281_441-279delinsCCT
ENST00000567675.1:n.76-281_76-279delinsCCT
NM_005576.2:c.1603-281_1603-279delinsCCT	NP_005567.2:n.1603-281_1603-279delinsCCT
XR_931824.1:n.2120-281_2120-279delinsCCT
NM_005576.3:c.1603-281_1603-279delinsCCT	NP_005567.2:n.1603-281_1603-279delinsCCT
XM_017022179.1:c.556-281_556-279delinsCCT	XP_016877668.1:n.556-281_556-279delinsCCT
XR_931824.2:n.2109-281_2109-279delinsCCT
NM_005576.4:c.1603-281_1603-279delinsCCT MANE Select	NP_005567.2:n.1603-281_1603-279delinsCCT