Canonical Allele Identifier: CA393104846
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.74220062A>C (hg19) chr15:g.73927721A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927721A>C , CM000677.2:g.73927721A>C GRCh38
NC_000015.9:g.74220062A>C , CM000677.1:g.74220062A>C GRCh37
NC_000015.8:g.72007115A>C NCBI36
NG_011466.1:g.6274A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.938A>C (LOXL1) MANE Select ENSP00000261921.7:p.Tyr313Ser
ENST00000261921.7:c.938A>C (LOXL1) ENSP00000261921.7:p.Tyr313Ser
ENST00000566011.5:c.938A>C (LOXL1) ENSP00000457827.1:p.Tyr313Ser
NM_005576.2:c.938A>C (LOXL1) NP_005567.2:p.Tyr313Ser
NR_040066.1:n.66T>G (LOXL1-AS1)
NR_040067.1:n.66T>G (LOXL1-AS1)
NR_040068.1:n.184+344T>G (LOXL1-AS1)
NR_040069.1:n.184+344T>G (LOXL1-AS1)
NR_040070.1:n.184+56T>G (LOXL1-AS1)
XM_011521555.1:c.938A>C (LOXL1) XP_011519857.1:p.Tyr313Ser
XR_931824.1:n.1271A>C (LOXL1)
NM_005576.3:c.938A>C (LOXL1) NP_005567.2:p.Tyr313Ser
XM_011521555.2:c.938A>C (LOXL1) XP_011519857.1:p.Tyr313Ser
XR_931824.2:n.1260A>C (LOXL1)
NM_005576.4:c.938A>C (LOXL1) MANE Select NP_005567.2:p.Tyr313Ser
Search 100 bp 5'
Search 100 bp 3'