Canonical Allele Identifier: CA715624024
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs1397109822

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949169A>T , CM000677.2:g.73949169A>T GRCh38
NC_000015.9:g.74241510A>T , CM000677.1:g.74241510A>T GRCh37
NC_000015.8:g.72028563A>T NCBI36
NG_011466.1:g.27722A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1603-290A>T MANE Select ENSP00000261921.7:n.1603-290A>T
ENST00000261921.7:c.1603-290A>T ENSP00000261921.7:n.1603-290A>T
ENST00000562548.1:n.688-290A>T
ENST00000566011.5:c.*491-290A>T ENSP00000457827.1:n.*491-290A>T
ENST00000566530.1:n.441-290A>T
ENST00000567675.1:n.76-290A>T
NM_005576.2:c.1603-290A>T NP_005567.2:n.1603-290A>T
XR_931824.1:n.2120-290A>T
NM_005576.3:c.1603-290A>T NP_005567.2:n.1603-290A>T
XM_017022179.1:c.556-290A>T XP_016877668.1:n.556-290A>T
XR_931824.2:n.2109-290A>T
NM_005576.4:c.1603-290A>T MANE Select NP_005567.2:n.1603-290A>T