Canonical Allele Identifier: CA491481295
Gene: LOXL1 HGNC NCBI
LOXL1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.74219457G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73927116G>C , CM000677.2:g.73927116G>C GRCh38
NC_000015.9:g.74219457G>C , CM000677.1:g.74219457G>C GRCh37
NC_000015.8:g.72006510G>C NCBI36
NG_011466.1:g.5669G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261921.8:c.333G>C (LOXL1) MANE Select ENSP00000261921.7:p.Val111=
ENST00000261921.7:c.333G>C (LOXL1) ENSP00000261921.7:p.Val111=
ENST00000566011.5:c.333G>C (LOXL1) ENSP00000457827.1:p.Val111=
NM_005576.2:c.333G>C (LOXL1) NP_005567.2:p.Val111=
NR_040066.1:n.133+538C>G (LOXL1-AS1)
NR_040067.1:n.133+538C>G (LOXL1-AS1)
NR_040068.1:n.184+949C>G (LOXL1-AS1)
NR_040069.1:n.184+949C>G (LOXL1-AS1)
NR_040070.1:n.184+661C>G (LOXL1-AS1)
XM_011521555.1:c.333G>C (LOXL1) XP_011519857.1:p.Val111=
XR_931824.1:n.666G>C (LOXL1)
NM_005576.3:c.333G>C (LOXL1) NP_005567.2:p.Val111=
XM_011521555.2:c.333G>C (LOXL1) XP_011519857.1:p.Val111=
XR_931824.2:n.655G>C (LOXL1)
NM_005576.4:c.333G>C (LOXL1) MANE Select NP_005567.2:p.Val111=