Canonical Allele Identifier: CA393104706

Gene: LOXL1 LOXL1-AS1

Linked Data

• gnomAD v4: 15-73927654-C-A
• MyVariant Identifiers: chr15:g.74219995C>A (hg19) ; chr15:g.73927654C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73927654C>A , CM000677.2:g.73927654C>A	GRCh38
NC_000015.9:g.74219995C>A , CM000677.1:g.74219995C>A	GRCh37
NC_000015.8:g.72007048C>A	NCBI36
NG_011466.1:g.6207C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.871C>A (LOXL1) MANE Select	ENSP00000261921.7:p.Pro291Thr
ENST00000261921.7:c.871C>A (LOXL1)	ENSP00000261921.7:p.Pro291Thr
ENST00000566011.5:c.871C>A (LOXL1)	ENSP00000457827.1:p.Pro291Thr
NM_005576.2:c.871C>A (LOXL1)	NP_005567.2:p.Pro291Thr
NR_040066.1:n.133G>T (LOXL1-AS1)
NR_040067.1:n.133G>T (LOXL1-AS1)
NR_040068.1:n.184+411G>T (LOXL1-AS1)
NR_040069.1:n.184+411G>T (LOXL1-AS1)
NR_040070.1:n.184+123G>T (LOXL1-AS1)
XM_011521555.1:c.871C>A (LOXL1)	XP_011519857.1:p.Pro291Thr
XR_931824.1:n.1204C>A (LOXL1)
NM_005576.3:c.871C>A (LOXL1)	NP_005567.2:p.Pro291Thr
XM_011521555.2:c.871C>A (LOXL1)	XP_011519857.1:p.Pro291Thr
XR_931824.2:n.1193C>A (LOXL1)
NM_005576.4:c.871C>A (LOXL1) MANE Select	NP_005567.2:p.Pro291Thr