Canonical Allele Identifier: CA393104927
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927762C>G , CM000677.2:g.73927762C>G GRCh38
NC_000015.9:g.74220103C>G , CM000677.1:g.74220103C>G GRCh37
NC_000015.8:g.72007156C>G NCBI36
NG_011466.1:g.6315C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.979C>G (LOXL1) MANE Select ENSP00000261921.7:p.Leu327Val
ENST00000261921.7:c.979C>G (LOXL1) ENSP00000261921.7:p.Leu327Val
ENST00000566011.5:c.979C>G (LOXL1) ENSP00000457827.1:p.Leu327Val
NM_005576.2:c.979C>G (LOXL1) NP_005567.2:p.Leu327Val
NR_040066.1:n.25G>C (LOXL1-AS1)
NR_040067.1:n.25G>C (LOXL1-AS1)
NR_040068.1:n.184+303G>C (LOXL1-AS1)
NR_040069.1:n.184+303G>C (LOXL1-AS1)
NR_040070.1:n.184+15G>C (LOXL1-AS1)
XM_011521555.1:c.979C>G (LOXL1) XP_011519857.1:p.Leu327Val
XR_931824.1:n.1312C>G (LOXL1)
NM_005576.3:c.979C>G (LOXL1) NP_005567.2:p.Leu327Val
XM_011521555.2:c.979C>G (LOXL1) XP_011519857.1:p.Leu327Val
XR_931824.2:n.1301C>G (LOXL1)
NM_005576.4:c.979C>G (LOXL1) MANE Select NP_005567.2:p.Leu327Val