Canonical Allele Identifier: CA491481650
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2068596560
MyVariant Identifiers: chr15:g.74219988G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927647G>A , CM000677.2:g.73927647G>A GRCh38
NC_000015.9:g.74219988G>A , CM000677.1:g.74219988G>A GRCh37
NC_000015.8:g.72007041G>A NCBI36
NG_011466.1:g.6200G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.864G>A (LOXL1) MANE Select ENSP00000261921.7:p.Gln288=
ENST00000261921.7:c.864G>A (LOXL1) ENSP00000261921.7:p.Gln288=
ENST00000566011.5:c.864G>A (LOXL1) ENSP00000457827.1:p.Gln288=
NM_005576.2:c.864G>A (LOXL1) NP_005567.2:p.Gln288=
NR_040066.1:n.133+7C>T (LOXL1-AS1)
NR_040067.1:n.133+7C>T (LOXL1-AS1)
NR_040068.1:n.184+418C>T (LOXL1-AS1)
NR_040069.1:n.184+418C>T (LOXL1-AS1)
NR_040070.1:n.184+130C>T (LOXL1-AS1)
XM_011521555.1:c.864G>A (LOXL1) XP_011519857.1:p.Gln288=
XR_931824.1:n.1197G>A (LOXL1)
NM_005576.3:c.864G>A (LOXL1) NP_005567.2:p.Gln288=
XM_011521555.2:c.864G>A (LOXL1) XP_011519857.1:p.Gln288=
XR_931824.2:n.1186G>A (LOXL1)
NM_005576.4:c.864G>A (LOXL1) MANE Select NP_005567.2:p.Gln288=