Canonical Allele Identifier: CA971450646
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs2068767165

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949151T>G , CM000677.2:g.73949151T>G GRCh38
NC_000015.9:g.74241492T>G , CM000677.1:g.74241492T>G GRCh37
NC_000015.8:g.72028545T>G NCBI36
NG_011466.1:g.27704T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1603-308T>G MANE Select ENSP00000261921.7:n.1603-308T>G
ENST00000261921.7:c.1603-308T>G ENSP00000261921.7:n.1603-308T>G
ENST00000562548.1:n.688-308T>G
ENST00000566011.5:c.*491-308T>G ENSP00000457827.1:n.*491-308T>G
ENST00000566530.1:n.441-308T>G
ENST00000567675.1:n.76-308T>G
NM_005576.2:c.1603-308T>G NP_005567.2:n.1603-308T>G
XR_931824.1:n.2120-308T>G
NM_005576.3:c.1603-308T>G NP_005567.2:n.1603-308T>G
XM_017022179.1:c.556-308T>G XP_016877668.1:n.556-308T>G
XR_931824.2:n.2109-308T>G
NM_005576.4:c.1603-308T>G MANE Select NP_005567.2:n.1603-308T>G