Canonical Allele Identifier: CA2187454809
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs1302514065

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73929748G>T , CM000677.2:g.73929748G>T GRCh38
NC_000015.9:g.74222089G>T , CM000677.1:g.74222089G>T GRCh37
NC_000015.8:g.72009142G>T NCBI36
NG_011466.1:g.8301G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1102+1863G>T MANE Select ENSP00000261921.7:n.1102+1863G>T
ENST00000261921.7:c.1102+1863G>T ENSP00000261921.7:n.1102+1863G>T
ENST00000566011.5:c.1102+1863G>T ENSP00000457827.1:n.1102+1863G>T
NM_005576.2:c.1102+1863G>T NP_005567.2:n.1102+1863G>T
XM_011521555.1:c.1102+1863G>T XP_011519857.1:n.1102+1863G>T
XR_931824.1:n.1435+1863G>T
NM_005576.3:c.1102+1863G>T NP_005567.2:n.1102+1863G>T
XM_011521555.2:c.1102+1863G>T XP_011519857.1:n.1102+1863G>T
XR_931824.2:n.1424+1863G>T
NM_005576.4:c.1102+1863G>T MANE Select NP_005567.2:n.1102+1863G>T