Canonical Allele Identifier: CA2187457802

Gene: LOXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73936670_73936671delinsCA , CM000677.2:g.73936670_73936671delinsCA	GRCh38
NC_000015.9:g.74229011_74229012delinsCA , CM000677.1:g.74229011_74229012delinsCA	GRCh37
NC_000015.8:g.72016064_72016065delinsCA	NCBI36
NG_011466.1:g.15223_15224delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1103-6184_1103-6183delinsCA MANE Select	ENSP00000261921.7:n.1103-6184_1103-6183delinsCA
ENST00000261921.7:c.1103-6184_1103-6183delinsCA	ENSP00000261921.7:n.1103-6184_1103-6183delinsCA
ENST00000566011.5:c.1103-5205_1103-5204delinsCA	ENSP00000457827.1:n.1103-5205_1103-5204delinsCA
NM_005576.2:c.1103-6184_1103-6183delinsCA	NP_005567.2:n.1103-6184_1103-6183delinsCA
XM_011521555.1:c.1103-5205_1103-5204delinsCA	XP_011519857.1:n.1103-5205_1103-5204delinsCA
XR_931824.1:n.1436-5205_1436-5204delinsCA
NM_005576.3:c.1103-6184_1103-6183delinsCA	NP_005567.2:n.1103-6184_1103-6183delinsCA
XM_011521555.2:c.1103-5205_1103-5204delinsCA	XP_011519857.1:n.1103-5205_1103-5204delinsCA
XR_931824.2:n.1425-5205_1425-5204delinsCA
NM_005576.4:c.1103-6184_1103-6183delinsCA MANE Select	NP_005567.2:n.1103-6184_1103-6183delinsCA