Canonical Allele Identifier: CA2187454886
Gene: LOXL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73929954G= , CM000677.2:g.73929954G= GRCh38
NC_000015.9:g.74222295G= , CM000677.1:g.74222295G= GRCh37
NC_000015.8:g.72009348G= NCBI36
NG_011466.1:g.8507G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1102+2069G= MANE Select ENSP00000261921.7:n.1102+2069G=
ENST00000261921.7:c.1102+2069G= ENSP00000261921.7:n.1102+2069G=
ENST00000566011.5:c.1102+2069G= ENSP00000457827.1:n.1102+2069G=
NM_005576.2:c.1102+2069G= NP_005567.2:n.1102+2069G=
XM_011521555.1:c.1102+2069G= XP_011519857.1:n.1102+2069G=
XR_931824.1:n.1435+2069G=
NM_005576.3:c.1102+2069G= NP_005567.2:n.1102+2069G=
XM_011521555.2:c.1102+2069G= XP_011519857.1:n.1102+2069G=
XR_931824.2:n.1424+2069G=
NM_005576.4:c.1102+2069G= MANE Select NP_005567.2:n.1102+2069G=
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