Canonical Allele Identifier: CA491481727
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.74220024C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927683C>G , CM000677.2:g.73927683C>G GRCh38
NC_000015.9:g.74220024C>G , CM000677.1:g.74220024C>G GRCh37
NC_000015.8:g.72007077C>G NCBI36
NG_011466.1:g.6236C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261921.8:c.900C>G (LOXL1) MANE Select ENSP00000261921.7:p.Ala300=
ENST00000261921.7:c.900C>G (LOXL1) ENSP00000261921.7:p.Ala300=
ENST00000566011.5:c.900C>G (LOXL1) ENSP00000457827.1:p.Ala300=
NM_005576.2:c.900C>G (LOXL1) NP_005567.2:p.Ala300=
NR_040066.1:n.104G>C (LOXL1-AS1)
NR_040067.1:n.104G>C (LOXL1-AS1)
NR_040068.1:n.184+382G>C (LOXL1-AS1)
NR_040069.1:n.184+382G>C (LOXL1-AS1)
NR_040070.1:n.184+94G>C (LOXL1-AS1)
XM_011521555.1:c.900C>G (LOXL1) XP_011519857.1:p.Ala300=
XR_931824.1:n.1233C>G (LOXL1)
NM_005576.3:c.900C>G (LOXL1) NP_005567.2:p.Ala300=
XM_011521555.2:c.900C>G (LOXL1) XP_011519857.1:p.Ala300=
XR_931824.2:n.1222C>G (LOXL1)
NM_005576.4:c.900C>G (LOXL1) MANE Select NP_005567.2:p.Ala300=