Canonical Allele Identifier: CA2538941267
Gene: LOXL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73930688_73930689insGG , CM000677.2:g.73930688_73930689insGG GRCh38
NC_000015.9:g.74223029_74223030insGG , CM000677.1:g.74223029_74223030insGG GRCh37
NC_000015.8:g.72010082_72010083insGG NCBI36
NG_011466.1:g.9241_9242insGG

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1102+2803_1102+2804insGG MANE Select ENSP00000261921.7:n.1102+2803_1102+2804in...
ENST00000261921.7:c.1102+2803_1102+2804insGG ENSP00000261921.7:n.1102+2803_1102+2804in...
ENST00000566011.5:c.1102+2803_1102+2804insGG ENSP00000457827.1:n.1102+2803_1102+2804in...
NM_005576.2:c.1102+2803_1102+2804insGG NP_005567.2:n.1102+2803_1102+2804insGG
XM_011521555.1:c.1102+2803_1102+2804insGG XP_011519857.1:n.1102+2803_1102+2804insGG...
XR_931824.1:n.1435+2803_1435+2804insGG
NM_005576.3:c.1102+2803_1102+2804insGG NP_005567.2:n.1102+2803_1102+2804insGG
XM_011521555.2:c.1102+2803_1102+2804insGG XP_011519857.1:n.1102+2803_1102+2804insGG...
XR_931824.2:n.1424+2803_1424+2804insGG
NM_005576.4:c.1102+2803_1102+2804insGG MANE Select NP_005567.2:n.1102+2803_1102+2804insGG
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