Canonical Allele Identifier: CA491481598
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.74220093G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927752G>A , CM000677.2:g.73927752G>A GRCh38
NC_000015.9:g.74220093G>A , CM000677.1:g.74220093G>A GRCh37
NC_000015.8:g.72007146G>A NCBI36
NG_011466.1:g.6305G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.969G>A (LOXL1) MANE Select ENSP00000261921.7:p.Pro323=
ENST00000261921.7:c.969G>A (LOXL1) ENSP00000261921.7:p.Pro323=
ENST00000566011.5:c.969G>A (LOXL1) ENSP00000457827.1:p.Pro323=
NM_005576.2:c.969G>A (LOXL1) NP_005567.2:p.Pro323=
NR_040066.1:n.35C>T (LOXL1-AS1)
NR_040067.1:n.35C>T (LOXL1-AS1)
NR_040068.1:n.184+313C>T (LOXL1-AS1)
NR_040069.1:n.184+313C>T (LOXL1-AS1)
NR_040070.1:n.184+25C>T (LOXL1-AS1)
XM_011521555.1:c.969G>A (LOXL1) XP_011519857.1:p.Pro323=
XR_931824.1:n.1302G>A (LOXL1)
NM_005576.3:c.969G>A (LOXL1) NP_005567.2:p.Pro323=
XM_011521555.2:c.969G>A (LOXL1) XP_011519857.1:p.Pro323=
XR_931824.2:n.1291G>A (LOXL1)
NM_005576.4:c.969G>A (LOXL1) MANE Select NP_005567.2:p.Pro323=