Canonical Allele Identifier: CA393103566
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927114G>T , CM000677.2:g.73927114G>T GRCh38
NC_000015.9:g.74219455G>T , CM000677.1:g.74219455G>T GRCh37
NC_000015.8:g.72006508G>T NCBI36
NG_011466.1:g.5667G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.331G>T (LOXL1) MANE Select ENSP00000261921.7:p.Val111Leu
ENST00000261921.7:c.331G>T (LOXL1) ENSP00000261921.7:p.Val111Leu
ENST00000566011.5:c.331G>T (LOXL1) ENSP00000457827.1:p.Val111Leu
NM_005576.2:c.331G>T (LOXL1) NP_005567.2:p.Val111Leu
NR_040066.1:n.133+540C>A (LOXL1-AS1)
NR_040067.1:n.133+540C>A (LOXL1-AS1)
NR_040068.1:n.184+951C>A (LOXL1-AS1)
NR_040069.1:n.184+951C>A (LOXL1-AS1)
NR_040070.1:n.184+663C>A (LOXL1-AS1)
XM_011521555.1:c.331G>T (LOXL1) XP_011519857.1:p.Val111Leu
XR_931824.1:n.664G>T (LOXL1)
NM_005576.3:c.331G>T (LOXL1) NP_005567.2:p.Val111Leu
XM_011521555.2:c.331G>T (LOXL1) XP_011519857.1:p.Val111Leu
XR_931824.2:n.653G>T (LOXL1)
NM_005576.4:c.331G>T (LOXL1) MANE Select NP_005567.2:p.Val111Leu