Canonical Allele Identifier: CA2187466159
Gene: LOXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949192A= , CM000677.2:g.73949192A= GRCh38
NC_000015.9:g.74241533A= , CM000677.1:g.74241533A= GRCh37
NC_000015.8:g.72028586A= NCBI36
NG_011466.1:g.27745A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1603-267A= MANE Select ENSP00000261921.7:n.1603-267A=
ENST00000261921.7:c.1603-267A= ENSP00000261921.7:n.1603-267A=
ENST00000562548.1:n.688-267A=
ENST00000566011.5:c.*491-267A= ENSP00000457827.1:n.*491-267A=
ENST00000566530.1:n.441-267A=
ENST00000567675.1:n.76-267A=
NM_005576.2:c.1603-267A= NP_005567.2:n.1603-267A=
XR_931824.1:n.2120-267A=
NM_005576.3:c.1603-267A= NP_005567.2:n.1603-267A=
XM_017022179.1:c.556-267A= XP_016877668.1:n.556-267A=
XR_931824.2:n.2109-267A=
NM_005576.4:c.1603-267A= MANE Select NP_005567.2:n.1603-267A=