Canonical Allele Identifier: CA2187463400
Gene: LOXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73946342G= , CM000677.2:g.73946342G= GRCh38
NC_000015.9:g.74238683G= , CM000677.1:g.74238683G= GRCh37
NC_000015.8:g.72025736G= NCBI36
NG_011466.1:g.24895G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1212-75G= MANE Select ENSP00000261921.7:n.1212-75G=
ENST00000261921.7:c.1212-75G= ENSP00000261921.7:n.1212-75G=
ENST00000566011.5:c.*100-75G= ENSP00000457827.1:n.*100-75G=
NM_005576.2:c.1212-75G= NP_005567.2:n.1212-75G=
XR_931824.1:n.1729-75G=
NM_005576.3:c.1212-75G= NP_005567.2:n.1212-75G=
XM_017022179.1:c.165-75G= XP_016877668.1:n.165-75G=
XR_931824.2:n.1718-75G=
NM_005576.4:c.1212-75G= MANE Select NP_005567.2:n.1212-75G=