Canonical Allele Identifier: CA491167260
Gene: LOXL1 HGNC NCBI

Linked Data

gnomAD v4: 15-73946435-G-A
MyVariant Identifiers: chr15:g.74238776G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73946435G>A , CM000677.2:g.73946435G>A GRCh38
NC_000015.9:g.74238776G>A , CM000677.1:g.74238776G>A GRCh37
NC_000015.8:g.72025829G>A NCBI36
NG_011466.1:g.24988G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1230G>A MANE Select ENSP00000261921.7:p.Glu410=
ENST00000261921.7:c.1230G>A ENSP00000261921.7:p.Glu410=
ENST00000566011.5:c.*118G>A ENSP00000457827.1:n.*118G>A
ENST00000566530.1:n.68G>A
NM_005576.2:c.1230G>A NP_005567.2:p.Glu410=
XR_931824.1:n.1747G>A
NM_005576.3:c.1230G>A NP_005567.2:p.Glu410=
XM_017022179.1:c.183G>A XP_016877668.1:p.Glu61=
XR_931824.2:n.1736G>A
NM_005576.4:c.1230G>A MANE Select NP_005567.2:p.Glu410=
Search 100 bp 5'
Search 100 bp 3'