Canonical Allele Identifier: CA393104732
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927666C>T , CM000677.2:g.73927666C>T GRCh38
NC_000015.9:g.74220007C>T , CM000677.1:g.74220007C>T GRCh37
NC_000015.8:g.72007060C>T NCBI36
NG_011466.1:g.6219C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.883C>T (LOXL1) MANE Select ENSP00000261921.7:p.Pro295Ser
ENST00000261921.7:c.883C>T (LOXL1) ENSP00000261921.7:p.Pro295Ser
ENST00000566011.5:c.883C>T (LOXL1) ENSP00000457827.1:p.Pro295Ser
NM_005576.2:c.883C>T (LOXL1) NP_005567.2:p.Pro295Ser
NR_040066.1:n.121G>A (LOXL1-AS1)
NR_040067.1:n.121G>A (LOXL1-AS1)
NR_040068.1:n.184+399G>A (LOXL1-AS1)
NR_040069.1:n.184+399G>A (LOXL1-AS1)
NR_040070.1:n.184+111G>A (LOXL1-AS1)
XM_011521555.1:c.883C>T (LOXL1) XP_011519857.1:p.Pro295Ser
XR_931824.1:n.1216C>T (LOXL1)
NM_005576.3:c.883C>T (LOXL1) NP_005567.2:p.Pro295Ser
XM_011521555.2:c.883C>T (LOXL1) XP_011519857.1:p.Pro295Ser
XR_931824.2:n.1205C>T (LOXL1)
NM_005576.4:c.883C>T (LOXL1) MANE Select NP_005567.2:p.Pro295Ser