Canonical Allele Identifier: CA2187453774
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927686T= , CM000677.2:g.73927686T= GRCh38
NC_000015.9:g.74220027T= , CM000677.1:g.74220027T= GRCh37
NC_000015.8:g.72007080T= NCBI36
NG_011466.1:g.6239T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.903T= (LOXL1) MANE Select ENSP00000261921.7:p.His301=
ENST00000261921.7:c.903T= (LOXL1) ENSP00000261921.7:p.His301=
ENST00000566011.5:c.903T= (LOXL1) ENSP00000457827.1:p.His301=
NM_005576.2:c.903T= (LOXL1) NP_005567.2:p.His301=
NR_040066.1:n.101A= (LOXL1-AS1)
NR_040067.1:n.101A= (LOXL1-AS1)
NR_040068.1:n.184+379A= (LOXL1-AS1)
NR_040069.1:n.184+379A= (LOXL1-AS1)
NR_040070.1:n.184+91A= (LOXL1-AS1)
XM_011521555.1:c.903T= (LOXL1) XP_011519857.1:p.His301=
XR_931824.1:n.1236T= (LOXL1)
NM_005576.3:c.903T= (LOXL1) NP_005567.2:p.His301=
XM_011521555.2:c.903T= (LOXL1) XP_011519857.1:p.His301=
XR_931824.2:n.1225T= (LOXL1)
NM_005576.4:c.903T= (LOXL1) MANE Select NP_005567.2:p.His301=