Canonical Allele Identifier: CA393103567
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927115T>G , CM000677.2:g.73927115T>G GRCh38
NC_000015.9:g.74219456T>G , CM000677.1:g.74219456T>G GRCh37
NC_000015.8:g.72006509T>G NCBI36
NG_011466.1:g.5668T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.332T>G (LOXL1) MANE Select ENSP00000261921.7:p.Val111Gly
ENST00000261921.7:c.332T>G (LOXL1) ENSP00000261921.7:p.Val111Gly
ENST00000566011.5:c.332T>G (LOXL1) ENSP00000457827.1:p.Val111Gly
NM_005576.2:c.332T>G (LOXL1) NP_005567.2:p.Val111Gly
NR_040066.1:n.133+539A>C (LOXL1-AS1)
NR_040067.1:n.133+539A>C (LOXL1-AS1)
NR_040068.1:n.184+950A>C (LOXL1-AS1)
NR_040069.1:n.184+950A>C (LOXL1-AS1)
NR_040070.1:n.184+662A>C (LOXL1-AS1)
XM_011521555.1:c.332T>G (LOXL1) XP_011519857.1:p.Val111Gly
XR_931824.1:n.665T>G (LOXL1)
NM_005576.3:c.332T>G (LOXL1) NP_005567.2:p.Val111Gly
XM_011521555.2:c.332T>G (LOXL1) XP_011519857.1:p.Val111Gly
XR_931824.2:n.654T>G (LOXL1)
NM_005576.4:c.332T>G (LOXL1) MANE Select NP_005567.2:p.Val111Gly