Canonical Allele Identifier: CA715615485

Gene: LOXL1

Linked Data

• dbSNP Id: rs1277643938
• MyVariant Identifiers: chr15:g.74222081T>C (hg19) ; chr15:g.73929740T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73929740T>C , CM000677.2:g.73929740T>C	GRCh38
NC_000015.9:g.74222081T>C , CM000677.1:g.74222081T>C	GRCh37
NC_000015.8:g.72009134T>C	NCBI36
NG_011466.1:g.8293T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.1102+1855T>C MANE Select	ENSP00000261921.7:n.1102+1855T>C
ENST00000261921.7:c.1102+1855T>C	ENSP00000261921.7:n.1102+1855T>C
ENST00000566011.5:c.1102+1855T>C	ENSP00000457827.1:n.1102+1855T>C
NM_005576.2:c.1102+1855T>C	NP_005567.2:n.1102+1855T>C
XM_011521555.1:c.1102+1855T>C	XP_011519857.1:n.1102+1855T>C
XR_931824.1:n.1435+1855T>C
NM_005576.3:c.1102+1855T>C	NP_005567.2:n.1102+1855T>C
XM_011521555.2:c.1102+1855T>C	XP_011519857.1:n.1102+1855T>C
XR_931824.2:n.1424+1855T>C
NM_005576.4:c.1102+1855T>C MANE Select	NP_005567.2:n.1102+1855T>C