Canonical Allele Identifier: CA715624005

Gene: LOXL1

Linked Data

• dbSNP Id: rs1314671488
• MyVariant Identifiers: chr15:g.74241464_74241476del (hg19) ; chr15:g.73949123_73949135del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73949125_73949137del , CM000677.2:g.73949125_73949137del	GRCh38
NC_000015.9:g.74241466_74241478del , CM000677.1:g.74241466_74241478del	GRCh37
NC_000015.8:g.72028519_72028531del	NCBI36
NG_011466.1:g.27678_27690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1603-334_1603-322del MANE Select	ENSP00000261921.7:n.1603-334_1603-322del
ENST00000261921.7:c.1603-334_1603-322del	ENSP00000261921.7:n.1603-334_1603-322del
ENST00000562548.1:n.688-334_688-322del
ENST00000566011.5:c.*491-334_*491-322del	ENSP00000457827.1:n.*491-334_*491-322del
ENST00000566530.1:n.441-334_441-322del
ENST00000567675.1:n.76-334_76-322del
NM_005576.2:c.1603-334_1603-322del	NP_005567.2:n.1603-334_1603-322del
XR_931824.1:n.2120-334_2120-322del
NM_005576.3:c.1603-334_1603-322del	NP_005567.2:n.1603-334_1603-322del
XM_017022179.1:c.556-334_556-322del	XP_016877668.1:n.556-334_556-322del
XR_931824.2:n.2109-334_2109-322del
NM_005576.4:c.1603-334_1603-322del MANE Select	NP_005567.2:n.1603-334_1603-322del