Canonical Allele Identifier: CA272712875

Gene: LOXL1

Linked Data

• dbSNP Id: rs571556026
• gnomAD v3: 15-73929991-T-A
• gnomAD v4: 15-73929991-T-A
• MyVariant Identifiers: chr15:g.74222332T>A (hg19) ; chr15:g.73929991T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929991T>A , CM000677.2:g.73929991T>A	GRCh38
NC_000015.9:g.74222332T>A , CM000677.1:g.74222332T>A	GRCh37
NC_000015.8:g.72009385T>A	NCBI36
NG_011466.1:g.8544T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.1102+2106T>A MANE Select	ENSP00000261921.7:n.1102+2106T>A
ENST00000261921.7:c.1102+2106T>A	ENSP00000261921.7:n.1102+2106T>A
ENST00000566011.5:c.1102+2106T>A	ENSP00000457827.1:n.1102+2106T>A
NM_005576.2:c.1102+2106T>A	NP_005567.2:n.1102+2106T>A
XM_011521555.1:c.1102+2106T>A	XP_011519857.1:n.1102+2106T>A
XR_931824.1:n.1435+2106T>A
NM_005576.3:c.1102+2106T>A	NP_005567.2:n.1102+2106T>A
XM_011521555.2:c.1102+2106T>A	XP_011519857.1:n.1102+2106T>A
XR_931824.2:n.1424+2106T>A
NM_005576.4:c.1102+2106T>A MANE Select	NP_005567.2:n.1102+2106T>A