Canonical Allele Identifier: CA14086265
Gene: LOXL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73936854G>A , CM000677.2:g.73936854G>A GRCh38
NC_000015.9:g.74229195G>A , CM000677.1:g.74229195G>A GRCh37
NC_000015.8:g.72016248G>A NCBI36
NG_011466.1:g.15407G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1103-6000G>A MANE Select ENSP00000261921.7:n.1103-6000G>A
ENST00000261921.7:c.1103-6000G>A ENSP00000261921.7:n.1103-6000G>A
ENST00000566011.5:c.1103-5021G>A ENSP00000457827.1:n.1103-5021G>A
NM_005576.2:c.1103-6000G>A NP_005567.2:n.1103-6000G>A
XM_011521555.1:c.1103-5021G>A XP_011519857.1:n.1103-5021G>A
XR_931824.1:n.1436-5021G>A
NM_005576.3:c.1103-6000G>A NP_005567.2:n.1103-6000G>A
XM_011521555.2:c.1103-5021G>A XP_011519857.1:n.1103-5021G>A
XR_931824.2:n.1425-5021G>A
NM_005576.4:c.1103-6000G>A MANE Select NP_005567.2:n.1103-6000G>A
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