Canonical Allele Identifier: CA2187457851
Gene: LOXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73936756T= , CM000677.2:g.73936756T= GRCh38
NC_000015.9:g.74229097T= , CM000677.1:g.74229097T= GRCh37
NC_000015.8:g.72016150T= NCBI36
NG_011466.1:g.15309T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1103-6098T= MANE Select ENSP00000261921.7:n.1103-6098T=
ENST00000261921.7:c.1103-6098T= ENSP00000261921.7:n.1103-6098T=
ENST00000566011.5:c.1103-5119T= ENSP00000457827.1:n.1103-5119T=
NM_005576.2:c.1103-6098T= NP_005567.2:n.1103-6098T=
XM_011521555.1:c.1103-5119T= XP_011519857.1:n.1103-5119T=
XR_931824.1:n.1436-5119T=
NM_005576.3:c.1103-6098T= NP_005567.2:n.1103-6098T=
XM_011521555.2:c.1103-5119T= XP_011519857.1:n.1103-5119T=
XR_931824.2:n.1425-5119T=
NM_005576.4:c.1103-6098T= MANE Select NP_005567.2:n.1103-6098T=