Canonical Allele Identifier: CA2187453346
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927117_73927118delinsCG , CM000677.2:g.73927117_73927118delinsCG GRCh38
NC_000015.9:g.74219458_74219459delinsCG , CM000677.1:g.74219458_74219459delinsCG GRCh37
NC_000015.8:g.72006511_72006512delinsCG NCBI36
NG_011466.1:g.5670_5671delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.334_335delinsCG (LOXL1) MANE Select ENSP00000261921.7:p.Arg112=
ENST00000261921.7:c.334_335delinsCG (LOXL1) ENSP00000261921.7:p.Arg112=
ENST00000566011.5:c.334_335delinsCG (LOXL1) ENSP00000457827.1:p.Arg112=
NM_005576.2:c.334_335delinsCG (LOXL1) NP_005567.2:p.Arg112=
NR_040066.1:n.133+536_133+537delinsCG (LOXL1-AS1)
NR_040067.1:n.133+536_133+537delinsCG (LOXL1-AS1)
NR_040068.1:n.184+947_184+948delinsCG (LOXL1-AS1)
NR_040069.1:n.184+947_184+948delinsCG (LOXL1-AS1)
NR_040070.1:n.184+659_184+660delinsCG (LOXL1-AS1)
XM_011521555.1:c.334_335delinsCG (LOXL1) XP_011519857.1:p.Arg112=
XR_931824.1:n.667_668delinsCG (LOXL1)
NM_005576.3:c.334_335delinsCG (LOXL1) NP_005567.2:p.Arg112=
XM_011521555.2:c.334_335delinsCG (LOXL1) XP_011519857.1:p.Arg112=
XR_931824.2:n.656_657delinsCG (LOXL1)
NM_005576.4:c.334_335delinsCG (LOXL1) MANE Select NP_005567.2:p.Arg112=