Canonical Allele Identifier: CA2562421375

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73936679_73936680insCCCTAATCTCTT , CM000677.2:g.73936679_73936680insCCCTAATCTCTT	GRCh38
NC_000015.9:g.74229020_74229021insCCCTAATCTCTT , CM000677.1:g.74229020_74229021insCCCTAATCTCTT	GRCh37
NC_000015.8:g.72016073_72016074insCCCTAATCTCTT	NCBI36
NG_011466.1:g.15232_15233insCCCTAATCTCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.1103-6175_1103-6174insCCCTAATCTCTT MANE Select	ENSP00000261921.7:n.1103-6175_1103-6174insCCCTAATCTCTT
ENST00000261921.7:c.1103-6175_1103-6174insCCCTAATCTCTT	ENSP00000261921.7:n.1103-6175_1103-6174insCCCTAATCTCTT
ENST00000566011.5:c.1103-5196_1103-5195insCCCTAATCTCTT	ENSP00000457827.1:n.1103-5196_1103-5195insCCCTAATCTCTT
NM_005576.2:c.1103-6175_1103-6174insCCCTAATCTCTT	NP_005567.2:n.1103-6175_1103-6174insCCCTAATCTCTT
XM_011521555.1:c.1103-5196_1103-5195insCCCTAATCTCTT	XP_011519857.1:n.1103-5196_1103-5195insCCCTAATCTCTT
XR_931824.1:n.1436-5196_1436-5195insCCCTAATCTCTT
NM_005576.3:c.1103-6175_1103-6174insCCCTAATCTCTT	NP_005567.2:n.1103-6175_1103-6174insCCCTAATCTCTT
XM_011521555.2:c.1103-5196_1103-5195insCCCTAATCTCTT	XP_011519857.1:n.1103-5196_1103-5195insCCCTAATCTCTT
XR_931824.2:n.1425-5196_1425-5195insCCCTAATCTCTT
NM_005576.4:c.1103-6175_1103-6174insCCCTAATCTCTT MANE Select	NP_005567.2:n.1103-6175_1103-6174insCCCTAATCTCTT