Canonical Allele Identifier: CA715615582

Gene: LOXL1

Linked Data

• dbSNP Id: rs1369769442
• MyVariant Identifiers: chr15:g.74222459A>T (hg19) ; chr15:g.73930118A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73930118A>T , CM000677.2:g.73930118A>T	GRCh38
NC_000015.9:g.74222459A>T , CM000677.1:g.74222459A>T	GRCh37
NC_000015.8:g.72009512A>T	NCBI36
NG_011466.1:g.8671A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1102+2233A>T MANE Select	ENSP00000261921.7:n.1102+2233A>T
ENST00000261921.7:c.1102+2233A>T	ENSP00000261921.7:n.1102+2233A>T
ENST00000566011.5:c.1102+2233A>T	ENSP00000457827.1:n.1102+2233A>T
NM_005576.2:c.1102+2233A>T	NP_005567.2:n.1102+2233A>T
XM_011521555.1:c.1102+2233A>T	XP_011519857.1:n.1102+2233A>T
XR_931824.1:n.1435+2233A>T
NM_005576.3:c.1102+2233A>T	NP_005567.2:n.1102+2233A>T
XM_011521555.2:c.1102+2233A>T	XP_011519857.1:n.1102+2233A>T
XR_931824.2:n.1424+2233A>T
NM_005576.4:c.1102+2233A>T MANE Select	NP_005567.2:n.1102+2233A>T