Canonical Allele Identifier: CA2187457859
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs2068676432

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73936765G>C , CM000677.2:g.73936765G>C GRCh38
NC_000015.9:g.74229106G>C , CM000677.1:g.74229106G>C GRCh37
NC_000015.8:g.72016159G>C NCBI36
NG_011466.1:g.15318G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1103-6089G>C MANE Select ENSP00000261921.7:n.1103-6089G>C
ENST00000261921.7:c.1103-6089G>C ENSP00000261921.7:n.1103-6089G>C
ENST00000566011.5:c.1103-5110G>C ENSP00000457827.1:n.1103-5110G>C
NM_005576.2:c.1103-6089G>C NP_005567.2:n.1103-6089G>C
XM_011521555.1:c.1103-5110G>C XP_011519857.1:n.1103-5110G>C
XR_931824.1:n.1436-5110G>C
NM_005576.3:c.1103-6089G>C NP_005567.2:n.1103-6089G>C
XM_011521555.2:c.1103-5110G>C XP_011519857.1:n.1103-5110G>C
XR_931824.2:n.1425-5110G>C
NM_005576.4:c.1103-6089G>C MANE Select NP_005567.2:n.1103-6089G>C