Canonical Allele Identifier: CA2187466177
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs2068767658

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949207del , CM000677.2:g.73949207del GRCh38
NC_000015.9:g.74241548del , CM000677.1:g.74241548del GRCh37
NC_000015.8:g.72028601del NCBI36
NG_011466.1:g.27760del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1603-252del MANE Select ENSP00000261921.7:n.1603-252del
ENST00000261921.7:c.1603-252del ENSP00000261921.7:n.1603-252del
ENST00000562548.1:n.688-252del
ENST00000566011.5:c.*491-252del ENSP00000457827.1:n.*491-252del
ENST00000566530.1:n.441-252del
ENST00000567675.1:n.76-252del
NM_005576.2:c.1603-252del NP_005567.2:n.1603-252del
XR_931824.1:n.2120-252del
NM_005576.3:c.1603-252del NP_005567.2:n.1603-252del
XM_017022179.1:c.556-252del XP_016877668.1:n.556-252del
XR_931824.2:n.2109-252del
NM_005576.4:c.1603-252del MANE Select NP_005567.2:n.1603-252del