Canonical Allele Identifier: CA2731192322
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs2141638492

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949136G>C , CM000677.2:g.73949136G>C GRCh38
NC_000015.9:g.74241477G>C , CM000677.1:g.74241477G>C GRCh37
NC_000015.8:g.72028530G>C NCBI36
NG_011466.1:g.27689G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1603-323G>C MANE Select ENSP00000261921.7:n.1603-323G>C
ENST00000261921.7:c.1603-323G>C ENSP00000261921.7:n.1603-323G>C
ENST00000562548.1:n.688-323G>C
ENST00000566011.5:c.*491-323G>C ENSP00000457827.1:n.*491-323G>C
ENST00000566530.1:n.441-323G>C
ENST00000567675.1:n.76-323G>C
NM_005576.2:c.1603-323G>C NP_005567.2:n.1603-323G>C
XR_931824.1:n.2120-323G>C
NM_005576.3:c.1603-323G>C NP_005567.2:n.1603-323G>C
XM_017022179.1:c.556-323G>C XP_016877668.1:n.556-323G>C
XR_931824.2:n.2109-323G>C
NM_005576.4:c.1603-323G>C MANE Select NP_005567.2:n.1603-323G>C