Canonical Allele Identifier: CA715624000
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs1231092510

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949120C>A , CM000677.2:g.73949120C>A GRCh38
NC_000015.9:g.74241461C>A , CM000677.1:g.74241461C>A GRCh37
NC_000015.8:g.72028514C>A NCBI36
NG_011466.1:g.27673C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1603-339C>A MANE Select ENSP00000261921.7:n.1603-339C>A
ENST00000261921.7:c.1603-339C>A ENSP00000261921.7:n.1603-339C>A
ENST00000562548.1:n.688-339C>A
ENST00000566011.5:c.*491-339C>A ENSP00000457827.1:n.*491-339C>A
ENST00000566530.1:n.441-339C>A
ENST00000567675.1:n.76-339C>A
NM_005576.2:c.1603-339C>A NP_005567.2:n.1603-339C>A
XR_931824.1:n.2120-339C>A
NM_005576.3:c.1603-339C>A NP_005567.2:n.1603-339C>A
XM_017022179.1:c.556-339C>A XP_016877668.1:n.556-339C>A
XR_931824.2:n.2109-339C>A
NM_005576.4:c.1603-339C>A MANE Select NP_005567.2:n.1603-339C>A