Canonical Allele Identifier: CA2187457792
Gene: LOXL1 HGNC NCBI

Linked Data

dbSNP Id: rs2068675149
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73936640A>G , CM000677.2:g.73936640A>G GRCh38
NC_000015.9:g.74228981A>G , CM000677.1:g.74228981A>G GRCh37
NC_000015.8:g.72016034A>G NCBI36
NG_011466.1:g.15193A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1103-6214A>G MANE Select ENSP00000261921.7:n.1103-6214A>G
ENST00000261921.7:c.1103-6214A>G ENSP00000261921.7:n.1103-6214A>G
ENST00000566011.5:c.1103-5235A>G ENSP00000457827.1:n.1103-5235A>G
NM_005576.2:c.1103-6214A>G NP_005567.2:n.1103-6214A>G
XM_011521555.1:c.1103-5235A>G XP_011519857.1:n.1103-5235A>G
XR_931824.1:n.1436-5235A>G
NM_005576.3:c.1103-6214A>G NP_005567.2:n.1103-6214A>G
XM_011521555.2:c.1103-5235A>G XP_011519857.1:n.1103-5235A>G
XR_931824.2:n.1425-5235A>G
NM_005576.4:c.1103-6214A>G MANE Select NP_005567.2:n.1103-6214A>G
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