Canonical Allele Identifier: CA2187457800
Gene: LOXL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73936670C= , CM000677.2:g.73936670C= GRCh38
NC_000015.9:g.74229011C= , CM000677.1:g.74229011C= GRCh37
NC_000015.8:g.72016064C= NCBI36
NG_011466.1:g.15223C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1103-6184C= MANE Select ENSP00000261921.7:n.1103-6184C=
ENST00000261921.7:c.1103-6184C= ENSP00000261921.7:n.1103-6184C=
ENST00000566011.5:c.1103-5205C= ENSP00000457827.1:n.1103-5205C=
NM_005576.2:c.1103-6184C= NP_005567.2:n.1103-6184C=
XM_011521555.1:c.1103-5205C= XP_011519857.1:n.1103-5205C=
XR_931824.1:n.1436-5205C=
NM_005576.3:c.1103-6184C= NP_005567.2:n.1103-6184C=
XM_011521555.2:c.1103-5205C= XP_011519857.1:n.1103-5205C=
XR_931824.2:n.1425-5205C=
NM_005576.4:c.1103-6184C= MANE Select NP_005567.2:n.1103-6184C=
Search 100 bp 5'
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