Canonical Allele Identifier: CA1578376288

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070110C= , CM000667.2:g.122070110C= GRCh38
NC_000005.9:g.121405805C= , CM000667.1:g.121405805C= GRCh37
NC_000005.8:g.121433704C= NCBI36
NG_008722.1:g.13251G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1190G= (LOX) MANE Select ENSP00000231004.4:p.Arg397=
ENST00000639739.2:c.*382G= (LOX) ENSP00000492324.2:n.*382G=
ENST00000231004.4:c.1190G= (LOX) ENSP00000231004.4:p.Arg397=
ENST00000503759.5:n.781G= (LOX)
ENST00000504881.1:n.312-5205C= (SRFBP1)
ENST00000505593.5:n.516G= (LOX)
ENST00000513319.5:n.533G= (LOX)
NM_001178102.1:c.500G= (LOX) NP_001171573.1:p.Arg167=
NM_001178102.2:c.500G= (LOX) NP_001171573.1:p.Arg167=
NM_001317073.1:c.299G= (LOX) NP_001304002.1:p.Arg100=
NM_002317.5:c.1190G= (LOX) NP_002308.2:p.Arg397=
NM_002317.6:c.1190G= (LOX) NP_002308.2:p.Arg397=
XM_017009111.2:c.1106-5205C= (SRFBP1) XP_016864600.2:n.1106-5205C=
NM_002317.7:c.1190G= (LOX) MANE Select NP_002308.2:p.Arg397=