Canonical Allele Identifier: CA491167261
Gene: LOXL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.74238779C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73946438C>A , CM000677.2:g.73946438C>A GRCh38
NC_000015.9:g.74238779C>A , CM000677.1:g.74238779C>A GRCh37
NC_000015.8:g.72025832C>A NCBI36
NG_011466.1:g.24991C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.1233C>A MANE Select ENSP00000261921.7:p.Ala411=
ENST00000261921.7:c.1233C>A ENSP00000261921.7:p.Ala411=
ENST00000566011.5:c.*121C>A ENSP00000457827.1:n.*121C>A
ENST00000566530.1:n.71C>A
NM_005576.2:c.1233C>A NP_005567.2:p.Ala411=
XR_931824.1:n.1750C>A
NM_005576.3:c.1233C>A NP_005567.2:p.Ala411=
XM_017022179.1:c.186C>A XP_016877668.1:p.Ala62=
XR_931824.2:n.1739C>A
NM_005576.4:c.1233C>A MANE Select NP_005567.2:p.Ala411=
Search 100 bp 5'
Search 100 bp 3'