Canonical Allele Identifier: CA2187466078
Gene: LOXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949076_73949078delinsCAG , CM000677.2:g.73949076_73949078delinsCAG GRCh38
NC_000015.9:g.74241417_74241419delinsCAG , CM000677.1:g.74241417_74241419delinsCAG GRCh37
NC_000015.8:g.72028470_72028472delinsCAG NCBI36
NG_011466.1:g.27629_27631delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1603-383_1603-381delinsCAG MANE Select ENSP00000261921.7:n.1603-383_1603-381delinsCAG
ENST00000261921.7:c.1603-383_1603-381delinsCAG ENSP00000261921.7:n.1603-383_1603-381delinsCAG
ENST00000562548.1:n.688-383_688-381delinsCAG
ENST00000566011.5:c.*491-383_*491-381delinsCAG ENSP00000457827.1:n.*491-383_*491-381delinsCAG
ENST00000566530.1:n.441-383_441-381delinsCAG
ENST00000567675.1:n.76-383_76-381delinsCAG
NM_005576.2:c.1603-383_1603-381delinsCAG NP_005567.2:n.1603-383_1603-381delinsCAG
XR_931824.1:n.2120-383_2120-381delinsCAG
NM_005576.3:c.1603-383_1603-381delinsCAG NP_005567.2:n.1603-383_1603-381delinsCAG
XM_017022179.1:c.556-383_556-381delinsCAG XP_016877668.1:n.556-383_556-381delinsCAG
XR_931824.2:n.2109-383_2109-381delinsCAG
NM_005576.4:c.1603-383_1603-381delinsCAG MANE Select NP_005567.2:n.1603-383_1603-381delinsCAG