Canonical Allele Identifier: CA360880215

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070101A>C , CM000667.2:g.122070101A>C GRCh38
NC_000005.9:g.121405796A>C , CM000667.1:g.121405796A>C GRCh37
NC_000005.8:g.121433695A>C NCBI36
NG_008722.1:g.13260T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1199T>G (LOX) MANE Select ENSP00000231004.4:p.Ile400Ser
ENST00000639739.2:c.*391T>G (LOX) ENSP00000492324.2:n.*391T>G
ENST00000231004.4:c.1199T>G (LOX) ENSP00000231004.4:p.Ile400Ser
ENST00000503759.5:n.790T>G (LOX)
ENST00000504881.1:n.312-5214A>C (SRFBP1)
ENST00000505593.5:n.525T>G (LOX)
ENST00000513319.5:n.542T>G (LOX)
NM_001178102.1:c.509T>G (LOX) NP_001171573.1:p.Ile170Ser
NM_001178102.2:c.509T>G (LOX) NP_001171573.1:p.Ile170Ser
NM_001317073.1:c.308T>G (LOX) NP_001304002.1:p.Ile103Ser
NM_002317.5:c.1199T>G (LOX) NP_002308.2:p.Ile400Ser
NM_002317.6:c.1199T>G (LOX) NP_002308.2:p.Ile400Ser
XM_017009111.2:c.1106-5214A>C (SRFBP1) XP_016864600.2:n.1106-5214A>C
NM_002317.7:c.1199T>G (LOX) MANE Select NP_002308.2:p.Ile400Ser