Canonical Allele Identifier: CA393104782

Gene: LOXL1 LOXL1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.74220031G>C (hg19) ; chr15:g.73927690G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73927690G>C , CM000677.2:g.73927690G>C	GRCh38
NC_000015.9:g.74220031G>C , CM000677.1:g.74220031G>C	GRCh37
NC_000015.8:g.72007084G>C	NCBI36
NG_011466.1:g.6243G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261921.8:c.907G>C (LOXL1) MANE Select	ENSP00000261921.7:p.Gly303Arg
ENST00000261921.7:c.907G>C (LOXL1)	ENSP00000261921.7:p.Gly303Arg
ENST00000566011.5:c.907G>C (LOXL1)	ENSP00000457827.1:p.Gly303Arg
NM_005576.2:c.907G>C (LOXL1)	NP_005567.2:p.Gly303Arg
NR_040066.1:n.97C>G (LOXL1-AS1)
NR_040067.1:n.97C>G (LOXL1-AS1)
NR_040068.1:n.184+375C>G (LOXL1-AS1)
NR_040069.1:n.184+375C>G (LOXL1-AS1)
NR_040070.1:n.184+87C>G (LOXL1-AS1)
XM_011521555.1:c.907G>C (LOXL1)	XP_011519857.1:p.Gly303Arg
XR_931824.1:n.1240G>C (LOXL1)
NM_005576.3:c.907G>C (LOXL1)	NP_005567.2:p.Gly303Arg
XM_011521555.2:c.907G>C (LOXL1)	XP_011519857.1:p.Gly303Arg
XR_931824.2:n.1229G>C (LOXL1)
NM_005576.4:c.907G>C (LOXL1) MANE Select	NP_005567.2:p.Gly303Arg