Canonical Allele Identifier: CA1578376282

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070094G= , CM000667.2:g.122070094G= GRCh38
NC_000005.9:g.121405789G= , CM000667.1:g.121405789G= GRCh37
NC_000005.8:g.121433688G= NCBI36
NG_008722.1:g.13267C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1206C= (LOX) MANE Select ENSP00000231004.4:p.Tyr402=
ENST00000639739.2:c.*398C= (LOX) ENSP00000492324.2:n.*398C=
ENST00000231004.4:c.1206C= (LOX) ENSP00000231004.4:p.Tyr402=
ENST00000503759.5:n.797C= (LOX)
ENST00000504881.1:n.312-5221G= (SRFBP1)
ENST00000505593.5:n.532C= (LOX)
ENST00000513319.5:n.549C= (LOX)
NM_001178102.1:c.516C= (LOX) NP_001171573.1:p.Tyr172=
NM_001178102.2:c.516C= (LOX) NP_001171573.1:p.Tyr172=
NM_001317073.1:c.315C= (LOX) NP_001304002.1:p.Tyr105=
NM_002317.5:c.1206C= (LOX) NP_002308.2:p.Tyr402=
NM_002317.6:c.1206C= (LOX) NP_002308.2:p.Tyr402=
XM_017009111.2:c.1106-5221G= (SRFBP1) XP_016864600.2:n.1106-5221G=
NM_002317.7:c.1206C= (LOX) MANE Select NP_002308.2:p.Tyr402=