Canonical Allele Identifier: CA393104902
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927748G>C , CM000677.2:g.73927748G>C GRCh38
NC_000015.9:g.74220089G>C , CM000677.1:g.74220089G>C GRCh37
NC_000015.8:g.72007142G>C NCBI36
NG_011466.1:g.6301G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.965G>C (LOXL1) MANE Select ENSP00000261921.7:p.Gly322Ala
ENST00000261921.7:c.965G>C (LOXL1) ENSP00000261921.7:p.Gly322Ala
ENST00000566011.5:c.965G>C (LOXL1) ENSP00000457827.1:p.Gly322Ala
NM_005576.2:c.965G>C (LOXL1) NP_005567.2:p.Gly322Ala
NR_040066.1:n.39C>G (LOXL1-AS1)
NR_040067.1:n.39C>G (LOXL1-AS1)
NR_040068.1:n.184+317C>G (LOXL1-AS1)
NR_040069.1:n.184+317C>G (LOXL1-AS1)
NR_040070.1:n.184+29C>G (LOXL1-AS1)
XM_011521555.1:c.965G>C (LOXL1) XP_011519857.1:p.Gly322Ala
XR_931824.1:n.1298G>C (LOXL1)
NM_005576.3:c.965G>C (LOXL1) NP_005567.2:p.Gly322Ala
XM_011521555.2:c.965G>C (LOXL1) XP_011519857.1:p.Gly322Ala
XR_931824.2:n.1287G>C (LOXL1)
NM_005576.4:c.965G>C (LOXL1) MANE Select NP_005567.2:p.Gly322Ala