Canonical Allele Identifier: CA393104765

Gene: LOXL1 LOXL1-AS1

Linked Data

• gnomAD v4: 15-73927681-G-T
• MyVariant Identifiers: chr15:g.74220022G>T (hg19) ; chr15:g.73927681G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73927681G>T , CM000677.2:g.73927681G>T	GRCh38
NC_000015.9:g.74220022G>T , CM000677.1:g.74220022G>T	GRCh37
NC_000015.8:g.72007075G>T	NCBI36
NG_011466.1:g.6234G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.898G>T (LOXL1) MANE Select	ENSP00000261921.7:p.Ala300Ser
ENST00000261921.7:c.898G>T (LOXL1)	ENSP00000261921.7:p.Ala300Ser
ENST00000566011.5:c.898G>T (LOXL1)	ENSP00000457827.1:p.Ala300Ser
NM_005576.2:c.898G>T (LOXL1)	NP_005567.2:p.Ala300Ser
NR_040066.1:n.106C>A (LOXL1-AS1)
NR_040067.1:n.106C>A (LOXL1-AS1)
NR_040068.1:n.184+384C>A (LOXL1-AS1)
NR_040069.1:n.184+384C>A (LOXL1-AS1)
NR_040070.1:n.184+96C>A (LOXL1-AS1)
XM_011521555.1:c.898G>T (LOXL1)	XP_011519857.1:p.Ala300Ser
XR_931824.1:n.1231G>T (LOXL1)
NM_005576.3:c.898G>T (LOXL1)	NP_005567.2:p.Ala300Ser
XM_011521555.2:c.898G>T (LOXL1)	XP_011519857.1:p.Ala300Ser
XR_931824.2:n.1220G>T (LOXL1)
NM_005576.4:c.898G>T (LOXL1) MANE Select	NP_005567.2:p.Ala300Ser