Canonical Allele Identifier: CA491481519
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

gnomAD v4: 15-73927725-C-A
MyVariant Identifiers: chr15:g.74220066C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927725C>A , CM000677.2:g.73927725C>A GRCh38
NC_000015.9:g.74220066C>A , CM000677.1:g.74220066C>A GRCh37
NC_000015.8:g.72007119C>A NCBI36
NG_011466.1:g.6278C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.942C>A (LOXL1) MANE Select ENSP00000261921.7:p.Ala314=
ENST00000261921.7:c.942C>A (LOXL1) ENSP00000261921.7:p.Ala314=
ENST00000566011.5:c.942C>A (LOXL1) ENSP00000457827.1:p.Ala314=
NM_005576.2:c.942C>A (LOXL1) NP_005567.2:p.Ala314=
NR_040066.1:n.62G>T (LOXL1-AS1)
NR_040067.1:n.62G>T (LOXL1-AS1)
NR_040068.1:n.184+340G>T (LOXL1-AS1)
NR_040069.1:n.184+340G>T (LOXL1-AS1)
NR_040070.1:n.184+52G>T (LOXL1-AS1)
XM_011521555.1:c.942C>A (LOXL1) XP_011519857.1:p.Ala314=
XR_931824.1:n.1275C>A (LOXL1)
NM_005576.3:c.942C>A (LOXL1) NP_005567.2:p.Ala314=
XM_011521555.2:c.942C>A (LOXL1) XP_011519857.1:p.Ala314=
XR_931824.2:n.1264C>A (LOXL1)
NM_005576.4:c.942C>A (LOXL1) MANE Select NP_005567.2:p.Ala314=
Search 100 bp 5'
Search 100 bp 3'