Canonical Allele Identifier: CA2187454881

Gene: LOXL1

Linked Data

• dbSNP Id: rs2068624230

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929941C>G , CM000677.2:g.73929941C>G	GRCh38
NC_000015.9:g.74222282C>G , CM000677.1:g.74222282C>G	GRCh37
NC_000015.8:g.72009335C>G	NCBI36
NG_011466.1:g.8494C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1102+2056C>G MANE Select	ENSP00000261921.7:n.1102+2056C>G
ENST00000261921.7:c.1102+2056C>G	ENSP00000261921.7:n.1102+2056C>G
ENST00000566011.5:c.1102+2056C>G	ENSP00000457827.1:n.1102+2056C>G
NM_005576.2:c.1102+2056C>G	NP_005567.2:n.1102+2056C>G
XM_011521555.1:c.1102+2056C>G	XP_011519857.1:n.1102+2056C>G
XR_931824.1:n.1435+2056C>G
NM_005576.3:c.1102+2056C>G	NP_005567.2:n.1102+2056C>G
XM_011521555.2:c.1102+2056C>G	XP_011519857.1:n.1102+2056C>G
XR_931824.2:n.1424+2056C>G
NM_005576.4:c.1102+2056C>G MANE Select	NP_005567.2:n.1102+2056C>G