Canonical Allele Identifier: CA971456483
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs2068624250

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73929943T>C , CM000677.2:g.73929943T>C GRCh38
NC_000015.9:g.74222284T>C , CM000677.1:g.74222284T>C GRCh37
NC_000015.8:g.72009337T>C NCBI36
NG_011466.1:g.8496T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1102+2058T>C MANE Select ENSP00000261921.7:n.1102+2058T>C
ENST00000261921.7:c.1102+2058T>C ENSP00000261921.7:n.1102+2058T>C
ENST00000566011.5:c.1102+2058T>C ENSP00000457827.1:n.1102+2058T>C
NM_005576.2:c.1102+2058T>C NP_005567.2:n.1102+2058T>C
XM_011521555.1:c.1102+2058T>C XP_011519857.1:n.1102+2058T>C
XR_931824.1:n.1435+2058T>C
NM_005576.3:c.1102+2058T>C NP_005567.2:n.1102+2058T>C
XM_011521555.2:c.1102+2058T>C XP_011519857.1:n.1102+2058T>C
XR_931824.2:n.1424+2058T>C
NM_005576.4:c.1102+2058T>C MANE Select NP_005567.2:n.1102+2058T>C