Canonical Allele Identifier: CA360880354

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070162C>A , CM000667.2:g.122070162C>A GRCh38
NC_000005.9:g.121405857C>A , CM000667.1:g.121405857C>A GRCh37
NC_000005.8:g.121433756C>A NCBI36
NG_008722.1:g.13199G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1138G>T (LOX) MANE Select ENSP00000231004.4:p.Val380Leu
ENST00000639739.2:c.*330G>T (LOX) ENSP00000492324.2:n.*330G>T
ENST00000231004.4:c.1138G>T (LOX) ENSP00000231004.4:p.Val380Leu
ENST00000503759.5:n.729G>T (LOX)
ENST00000504881.1:n.312-5153C>A (SRFBP1)
ENST00000505593.5:n.464G>T (LOX)
ENST00000513319.5:n.481G>T (LOX)
NM_001178102.1:c.448G>T (LOX) NP_001171573.1:p.Val150Leu
NM_001178102.2:c.448G>T (LOX) NP_001171573.1:p.Val150Leu
NM_001317073.1:c.247G>T (LOX) NP_001304002.1:p.Val83Leu
NM_002317.5:c.1138G>T (LOX) NP_002308.2:p.Val380Leu
NM_002317.6:c.1138G>T (LOX) NP_002308.2:p.Val380Leu
XM_017009111.2:c.1106-5153C>A (SRFBP1) XP_016864600.2:n.1106-5153C>A
NM_002317.7:c.1138G>T (LOX) MANE Select NP_002308.2:p.Val380Leu