Canonical Allele Identifier: CA2187453816
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927758C= , CM000677.2:g.73927758C= GRCh38
NC_000015.9:g.74220099C= , CM000677.1:g.74220099C= GRCh37
NC_000015.8:g.72007152C= NCBI36
NG_011466.1:g.6311C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.975C= (LOXL1) MANE Select ENSP00000261921.7:p.Arg325=
ENST00000261921.7:c.975C= (LOXL1) ENSP00000261921.7:p.Arg325=
ENST00000566011.5:c.975C= (LOXL1) ENSP00000457827.1:p.Arg325=
NM_005576.2:c.975C= (LOXL1) NP_005567.2:p.Arg325=
NR_040066.1:n.29G= (LOXL1-AS1)
NR_040067.1:n.29G= (LOXL1-AS1)
NR_040068.1:n.184+307G= (LOXL1-AS1)
NR_040069.1:n.184+307G= (LOXL1-AS1)
NR_040070.1:n.184+19G= (LOXL1-AS1)
XM_011521555.1:c.975C= (LOXL1) XP_011519857.1:p.Arg325=
XR_931824.1:n.1308C= (LOXL1)
NM_005576.3:c.975C= (LOXL1) NP_005567.2:p.Arg325=
XM_011521555.2:c.975C= (LOXL1) XP_011519857.1:p.Arg325=
XR_931824.2:n.1297C= (LOXL1)
NM_005576.4:c.975C= (LOXL1) MANE Select NP_005567.2:p.Arg325=