Canonical Allele Identifier: CA360880357

Linked Data

Genomic Alleles

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

Transcript Alleles

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