Canonical Allele Identifier: CA715624003
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs1357658931

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949122A>G , CM000677.2:g.73949122A>G GRCh38
NC_000015.9:g.74241463A>G , CM000677.1:g.74241463A>G GRCh37
NC_000015.8:g.72028516A>G NCBI36
NG_011466.1:g.27675A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1603-337A>G MANE Select ENSP00000261921.7:n.1603-337A>G
ENST00000261921.7:c.1603-337A>G ENSP00000261921.7:n.1603-337A>G
ENST00000562548.1:n.688-337A>G
ENST00000566011.5:c.*491-337A>G ENSP00000457827.1:n.*491-337A>G
ENST00000566530.1:n.441-337A>G
ENST00000567675.1:n.76-337A>G
NM_005576.2:c.1603-337A>G NP_005567.2:n.1603-337A>G
XR_931824.1:n.2120-337A>G
NM_005576.3:c.1603-337A>G NP_005567.2:n.1603-337A>G
XM_017022179.1:c.556-337A>G XP_016877668.1:n.556-337A>G
XR_931824.2:n.2109-337A>G
NM_005576.4:c.1603-337A>G MANE Select NP_005567.2:n.1603-337A>G