Canonical Allele Identifier: CA2187453780
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927701C= , CM000677.2:g.73927701C= GRCh38
NC_000015.9:g.74220042C= , CM000677.1:g.74220042C= GRCh37
NC_000015.8:g.72007095C= NCBI36
NG_011466.1:g.6254C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.918C= (LOXL1) MANE Select ENSP00000261921.7:p.Arg306=
ENST00000261921.7:c.918C= (LOXL1) ENSP00000261921.7:p.Arg306=
ENST00000566011.5:c.918C= (LOXL1) ENSP00000457827.1:p.Arg306=
NM_005576.2:c.918C= (LOXL1) NP_005567.2:p.Arg306=
NR_040066.1:n.86G= (LOXL1-AS1)
NR_040067.1:n.86G= (LOXL1-AS1)
NR_040068.1:n.184+364G= (LOXL1-AS1)
NR_040069.1:n.184+364G= (LOXL1-AS1)
NR_040070.1:n.184+76G= (LOXL1-AS1)
XM_011521555.1:c.918C= (LOXL1) XP_011519857.1:p.Arg306=
XR_931824.1:n.1251C= (LOXL1)
NM_005576.3:c.918C= (LOXL1) NP_005567.2:p.Arg306=
XM_011521555.2:c.918C= (LOXL1) XP_011519857.1:p.Arg306=
XR_931824.2:n.1240C= (LOXL1)
NM_005576.4:c.918C= (LOXL1) MANE Select NP_005567.2:p.Arg306=