Canonical Allele Identifier: CA7651607

Gene: LOXL1 LOXL1-AS1

Linked Data

• dbSNP Id: rs762375758
• ExAC: 15:74220022 G / A
• gnomAD v2: 15-74220022-G-A
• gnomAD v4: 15-73927681-G-A
• MyVariant Identifiers: chr15:g.74220022G>A (hg19) ; chr15:g.73927681G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.898G>A (LOXL1) MANE Select	ENSP00000261921.7:p.Ala300Thr
ENST00000261921.7:c.898G>A (LOXL1)	ENSP00000261921.7:p.Ala300Thr
ENST00000566011.5:c.898G>A (LOXL1)	ENSP00000457827.1:p.Ala300Thr
NM_005576.2:c.898G>A (LOXL1)	NP_005567.2:p.Ala300Thr
NR_040066.1:n.106C>T (LOXL1-AS1)
NR_040067.1:n.106C>T (LOXL1-AS1)
NR_040068.1:n.184+384C>T (LOXL1-AS1)
NR_040069.1:n.184+384C>T (LOXL1-AS1)
NR_040070.1:n.184+96C>T (LOXL1-AS1)
XM_011521555.1:c.898G>A (LOXL1)	XP_011519857.1:p.Ala300Thr
XR_931824.1:n.1231G>A (LOXL1)
NM_005576.3:c.898G>A (LOXL1)	NP_005567.2:p.Ala300Thr
XM_011521555.2:c.898G>A (LOXL1)	XP_011519857.1:p.Ala300Thr
XR_931824.2:n.1220G>A (LOXL1)
NM_005576.4:c.898G>A (LOXL1) MANE Select	NP_005567.2:p.Ala300Thr