Canonical Allele Identifier: CA393104712

Gene: LOXL1 LOXL1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.74219998G>C (hg19) ; chr15:g.73927657G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73927657G>C , CM000677.2:g.73927657G>C	GRCh38
NC_000015.9:g.74219998G>C , CM000677.1:g.74219998G>C	GRCh37
NC_000015.8:g.72007051G>C	NCBI36
NG_011466.1:g.6210G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.874G>C (LOXL1) MANE Select	ENSP00000261921.7:p.Asp292His
ENST00000261921.7:c.874G>C (LOXL1)	ENSP00000261921.7:p.Asp292His
ENST00000566011.5:c.874G>C (LOXL1)	ENSP00000457827.1:p.Asp292His
NM_005576.2:c.874G>C (LOXL1)	NP_005567.2:p.Asp292His
NR_040066.1:n.130C>G (LOXL1-AS1)
NR_040067.1:n.130C>G (LOXL1-AS1)
NR_040068.1:n.184+408C>G (LOXL1-AS1)
NR_040069.1:n.184+408C>G (LOXL1-AS1)
NR_040070.1:n.184+120C>G (LOXL1-AS1)
XM_011521555.1:c.874G>C (LOXL1)	XP_011519857.1:p.Asp292His
XR_931824.1:n.1207G>C (LOXL1)
NM_005576.3:c.874G>C (LOXL1)	NP_005567.2:p.Asp292His
XM_011521555.2:c.874G>C (LOXL1)	XP_011519857.1:p.Asp292His
XR_931824.2:n.1196G>C (LOXL1)
NM_005576.4:c.874G>C (LOXL1) MANE Select	NP_005567.2:p.Asp292His