Canonical Allele Identifier: CA272712725
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs978973425

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73929701C>T , CM000677.2:g.73929701C>T GRCh38
NC_000015.9:g.74222042C>T , CM000677.1:g.74222042C>T GRCh37
NC_000015.8:g.72009095C>T NCBI36
NG_011466.1:g.8254C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1102+1816C>T MANE Select ENSP00000261921.7:n.1102+1816C>T
ENST00000261921.7:c.1102+1816C>T ENSP00000261921.7:n.1102+1816C>T
ENST00000566011.5:c.1102+1816C>T ENSP00000457827.1:n.1102+1816C>T
NM_005576.2:c.1102+1816C>T NP_005567.2:n.1102+1816C>T
XM_011521555.1:c.1102+1816C>T XP_011519857.1:n.1102+1816C>T
XR_931824.1:n.1435+1816C>T
NM_005576.3:c.1102+1816C>T NP_005567.2:n.1102+1816C>T
XM_011521555.2:c.1102+1816C>T XP_011519857.1:n.1102+1816C>T
XR_931824.2:n.1424+1816C>T
NM_005576.4:c.1102+1816C>T MANE Select NP_005567.2:n.1102+1816C>T