Canonical Allele Identifier: CA1578376305

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070160T= , CM000667.2:g.122070160T= GRCh38
NC_000005.9:g.121405855T= , CM000667.1:g.121405855T= GRCh37
NC_000005.8:g.121433754T= NCBI36
NG_008722.1:g.13201A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1140A= (LOX) MANE Select ENSP00000231004.4:p.Val380=
ENST00000639739.2:c.*332A= (LOX) ENSP00000492324.2:n.*332A=
ENST00000231004.4:c.1140A= (LOX) ENSP00000231004.4:p.Val380=
ENST00000503759.5:n.731A= (LOX)
ENST00000504881.1:n.312-5155T= (SRFBP1)
ENST00000505593.5:n.466A= (LOX)
ENST00000513319.5:n.483A= (LOX)
NM_001178102.1:c.450A= (LOX) NP_001171573.1:p.Val150=
NM_001178102.2:c.450A= (LOX) NP_001171573.1:p.Val150=
NM_001317073.1:c.249A= (LOX) NP_001304002.1:p.Val83=
NM_002317.5:c.1140A= (LOX) NP_002308.2:p.Val380=
NM_002317.6:c.1140A= (LOX) NP_002308.2:p.Val380=
XM_017009111.2:c.1106-5155T= (SRFBP1) XP_016864600.2:n.1106-5155T=
NM_002317.7:c.1140A= (LOX) MANE Select NP_002308.2:p.Val380=