Canonical Allele Identifier: CA2187463553
Gene: LOXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73946437C= , CM000677.2:g.73946437C= GRCh38
NC_000015.9:g.74238778C= , CM000677.1:g.74238778C= GRCh37
NC_000015.8:g.72025831C= NCBI36
NG_011466.1:g.24990C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1232C= MANE Select ENSP00000261921.7:p.Ala411=
ENST00000261921.7:c.1232C= ENSP00000261921.7:p.Ala411=
ENST00000566011.5:c.*120C= ENSP00000457827.1:n.*120C=
ENST00000566530.1:n.70C=
NM_005576.2:c.1232C= NP_005567.2:p.Ala411=
XR_931824.1:n.1749C=
NM_005576.3:c.1232C= NP_005567.2:p.Ala411=
XM_017022179.1:c.185C= XP_016877668.1:p.Ala62=
XR_931824.2:n.1738C=
NM_005576.4:c.1232C= MANE Select NP_005567.2:p.Ala411=