Canonical Allele Identifier: CA2187466086
Gene: LOXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949077_73949078delinsAG , CM000677.2:g.73949077_73949078delinsAG GRCh38
NC_000015.9:g.74241418_74241419delinsAG , CM000677.1:g.74241418_74241419delinsAG GRCh37
NC_000015.8:g.72028471_72028472delinsAG NCBI36
NG_011466.1:g.27630_27631delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.1603-382_1603-381delinsAG MANE Select ENSP00000261921.7:n.1603-382_1603-381delinsAG
ENST00000261921.7:c.1603-382_1603-381delinsAG ENSP00000261921.7:n.1603-382_1603-381delinsAG
ENST00000562548.1:n.688-382_688-381delinsAG
ENST00000566011.5:c.*491-382_*491-381delinsAG ENSP00000457827.1:n.*491-382_*491-381delinsAG
ENST00000566530.1:n.441-382_441-381delinsAG
ENST00000567675.1:n.76-382_76-381delinsAG
NM_005576.2:c.1603-382_1603-381delinsAG NP_005567.2:n.1603-382_1603-381delinsAG
XR_931824.1:n.2120-382_2120-381delinsAG
NM_005576.3:c.1603-382_1603-381delinsAG NP_005567.2:n.1603-382_1603-381delinsAG
XM_017022179.1:c.556-382_556-381delinsAG XP_016877668.1:n.556-382_556-381delinsAG
XR_931824.2:n.2109-382_2109-381delinsAG
NM_005576.4:c.1603-382_1603-381delinsAG MANE Select NP_005567.2:n.1603-382_1603-381delinsAG