Canonical Allele Identifier: CA491481269
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.74219448G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927107G>A , CM000677.2:g.73927107G>A GRCh38
NC_000015.9:g.74219448G>A , CM000677.1:g.74219448G>A GRCh37
NC_000015.8:g.72006501G>A NCBI36
NG_011466.1:g.5660G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.324G>A (LOXL1) MANE Select ENSP00000261921.7:p.Ser108=
ENST00000261921.7:c.324G>A (LOXL1) ENSP00000261921.7:p.Ser108=
ENST00000566011.5:c.324G>A (LOXL1) ENSP00000457827.1:p.Ser108=
NM_005576.2:c.324G>A (LOXL1) NP_005567.2:p.Ser108=
NR_040066.1:n.133+547C>T (LOXL1-AS1)
NR_040067.1:n.133+547C>T (LOXL1-AS1)
NR_040068.1:n.184+958C>T (LOXL1-AS1)
NR_040069.1:n.184+958C>T (LOXL1-AS1)
NR_040070.1:n.184+670C>T (LOXL1-AS1)
XM_011521555.1:c.324G>A (LOXL1) XP_011519857.1:p.Ser108=
XR_931824.1:n.657G>A (LOXL1)
NM_005576.3:c.324G>A (LOXL1) NP_005567.2:p.Ser108=
XM_011521555.2:c.324G>A (LOXL1) XP_011519857.1:p.Ser108=
XR_931824.2:n.646G>A (LOXL1)
NM_005576.4:c.324G>A (LOXL1) MANE Select NP_005567.2:p.Ser108=