Canonical Allele Identifier: CA2187466084
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs1470688112
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73949077A>G , CM000677.2:g.73949077A>G GRCh38
NC_000015.9:g.74241418A>G , CM000677.1:g.74241418A>G GRCh37
NC_000015.8:g.72028471A>G NCBI36
NG_011466.1:g.27630A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1603-382A>G MANE Select ENSP00000261921.7:n.1603-382A>G
ENST00000261921.7:c.1603-382A>G ENSP00000261921.7:n.1603-382A>G
ENST00000562548.1:n.688-382A>G
ENST00000566011.5:c.*491-382A>G ENSP00000457827.1:n.*491-382A>G
ENST00000566530.1:n.441-382A>G
ENST00000567675.1:n.76-382A>G
NM_005576.2:c.1603-382A>G NP_005567.2:n.1603-382A>G
XR_931824.1:n.2120-382A>G
NM_005576.3:c.1603-382A>G NP_005567.2:n.1603-382A>G
XM_017022179.1:c.556-382A>G XP_016877668.1:n.556-382A>G
XR_931824.2:n.2109-382A>G
NM_005576.4:c.1603-382A>G MANE Select NP_005567.2:n.1603-382A>G
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