Canonical Allele Identifier: CA2187453779
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927700G= , CM000677.2:g.73927700G= GRCh38
NC_000015.9:g.74220041G= , CM000677.1:g.74220041G= GRCh37
NC_000015.8:g.72007094G= NCBI36
NG_011466.1:g.6253G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.917G= (LOXL1) MANE Select ENSP00000261921.7:p.Arg306=
ENST00000261921.7:c.917G= (LOXL1) ENSP00000261921.7:p.Arg306=
ENST00000566011.5:c.917G= (LOXL1) ENSP00000457827.1:p.Arg306=
NM_005576.2:c.917G= (LOXL1) NP_005567.2:p.Arg306=
NR_040066.1:n.87C= (LOXL1-AS1)
NR_040067.1:n.87C= (LOXL1-AS1)
NR_040068.1:n.184+365C= (LOXL1-AS1)
NR_040069.1:n.184+365C= (LOXL1-AS1)
NR_040070.1:n.184+77C= (LOXL1-AS1)
XM_011521555.1:c.917G= (LOXL1) XP_011519857.1:p.Arg306=
XR_931824.1:n.1250G= (LOXL1)
NM_005576.3:c.917G= (LOXL1) NP_005567.2:p.Arg306=
XM_011521555.2:c.917G= (LOXL1) XP_011519857.1:p.Arg306=
XR_931824.2:n.1239G= (LOXL1)
NM_005576.4:c.917G= (LOXL1) MANE Select NP_005567.2:p.Arg306=