Canonical Allele Identifier: CA360880358

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070163A>T , CM000667.2:g.122070163A>T GRCh38
NC_000005.9:g.121405858A>T , CM000667.1:g.121405858A>T GRCh37
NC_000005.8:g.121433757A>T NCBI36
NG_008722.1:g.13198T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1137T>A (LOX) MANE Select ENSP00000231004.4:p.Ser379Arg
ENST00000639739.2:c.*329T>A (LOX) ENSP00000492324.2:n.*329T>A
ENST00000231004.4:c.1137T>A (LOX) ENSP00000231004.4:p.Ser379Arg
ENST00000503759.5:n.728T>A (LOX)
ENST00000504881.1:n.312-5152A>T (SRFBP1)
ENST00000505593.5:n.463T>A (LOX)
ENST00000513319.5:n.480T>A (LOX)
NM_001178102.1:c.447T>A (LOX) NP_001171573.1:p.Ser149Arg
NM_001178102.2:c.447T>A (LOX) NP_001171573.1:p.Ser149Arg
NM_001317073.1:c.246T>A (LOX) NP_001304002.1:p.Ser82Arg
NM_002317.5:c.1137T>A (LOX) NP_002308.2:p.Ser379Arg
NM_002317.6:c.1137T>A (LOX) NP_002308.2:p.Ser379Arg
XM_017009111.2:c.1106-5152A>T (SRFBP1) XP_016864600.2:n.1106-5152A>T
NM_002317.7:c.1137T>A (LOX) MANE Select NP_002308.2:p.Ser379Arg