Canonical Allele Identifier: CA360880295

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070135A>T , CM000667.2:g.122070135A>T GRCh38
NC_000005.9:g.121405830A>T , CM000667.1:g.121405830A>T GRCh37
NC_000005.8:g.121433729A>T NCBI36
NG_008722.1:g.13226T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1165T>A (LOX) MANE Select ENSP00000231004.4:p.Ser389Thr
ENST00000639739.2:c.*357T>A (LOX) ENSP00000492324.2:n.*357T>A
ENST00000231004.4:c.1165T>A (LOX) ENSP00000231004.4:p.Ser389Thr
ENST00000503759.5:n.756T>A (LOX)
ENST00000504881.1:n.312-5180A>T (SRFBP1)
ENST00000505593.5:n.491T>A (LOX)
ENST00000513319.5:n.508T>A (LOX)
NM_001178102.1:c.475T>A (LOX) NP_001171573.1:p.Ser159Thr
NM_001178102.2:c.475T>A (LOX) NP_001171573.1:p.Ser159Thr
NM_001317073.1:c.274T>A (LOX) NP_001304002.1:p.Ser92Thr
NM_002317.5:c.1165T>A (LOX) NP_002308.2:p.Ser389Thr
NM_002317.6:c.1165T>A (LOX) NP_002308.2:p.Ser389Thr
XM_017009111.2:c.1106-5180A>T (SRFBP1) XP_016864600.2:n.1106-5180A>T
NM_002317.7:c.1165T>A (LOX) MANE Select NP_002308.2:p.Ser389Thr