Canonical Allele Identifier: CA2187463542
Gene: LOXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73946429C= , CM000677.2:g.73946429C= GRCh38
NC_000015.9:g.74238770C= , CM000677.1:g.74238770C= GRCh37
NC_000015.8:g.72025823C= NCBI36
NG_011466.1:g.24982C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1224C= MANE Select ENSP00000261921.7:p.Ala408=
ENST00000261921.7:c.1224C= ENSP00000261921.7:p.Ala408=
ENST00000566011.5:c.*112C= ENSP00000457827.1:n.*112C=
ENST00000566530.1:n.62C=
NM_005576.2:c.1224C= NP_005567.2:p.Ala408=
XR_931824.1:n.1741C=
NM_005576.3:c.1224C= NP_005567.2:p.Ala408=
XM_017022179.1:c.177C= XP_016877668.1:p.Ala59=
XR_931824.2:n.1730C=
NM_005576.4:c.1224C= MANE Select NP_005567.2:p.Ala408=