Canonical Allele Identifier: CA3383888

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122074062G>T , CM000667.2:g.122074062G>T GRCh38
NC_000005.9:g.121409757G>T , CM000667.1:g.121409757G>T GRCh37
NC_000005.8:g.121437656G>T NCBI36
NG_008722.1:g.9299C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.986C>A (LOX) MANE Select ENSP00000231004.4:p.Ser329Tyr
ENST00000639739.2:c.*178C>A (LOX) ENSP00000492324.2:n.*178C>A
ENST00000231004.4:c.986C>A (LOX) ENSP00000231004.4:p.Ser329Tyr
ENST00000503759.5:n.577C>A (LOX)
ENST00000504881.1:n.312-1253G>T (SRFBP1)
ENST00000505593.5:n.312C>A (LOX)
ENST00000508067.1:c.364C>A (LOX) ENSP00000427538.1:n.364C>A
ENST00000513319.5:n.329C>A (LOX)
NM_001178102.1:c.296C>A (LOX) NP_001171573.1:p.Ser99Tyr
NM_001178102.2:c.296C>A (LOX) NP_001171573.1:p.Ser99Tyr
NM_001317073.1:c.95C>A (LOX) NP_001304002.1:p.Ser32Tyr
NM_002317.5:c.986C>A (LOX) NP_002308.2:p.Ser329Tyr
NM_002317.6:c.986C>A (LOX) NP_002308.2:p.Ser329Tyr
XM_017009111.2:c.1106-1253G>T (SRFBP1) XP_016864600.2:n.1106-1253G>T
NM_002317.7:c.986C>A (LOX) MANE Select NP_002308.2:p.Ser329Tyr