Canonical Allele Identifier: CA2674996458

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070369dup , CM000667.2:g.122070369dup GRCh38
NC_000005.9:g.121406064dup , CM000667.1:g.121406064dup GRCh37
NC_000005.8:g.121433963dup NCBI36
NG_008722.1:g.12993dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1131+126dup (LOX) MANE Select ENSP00000231004.4:n.1131+126dup
ENST00000639739.2:c.*323+126dup (LOX) ENSP00000492324.2:n.*323+126dup
ENST00000231004.4:c.1131+126dup (LOX) ENSP00000231004.4:n.1131+126dup
ENST00000503759.5:n.722+126dup (LOX)
ENST00000504881.1:n.312-4946dup (SRFBP1)
ENST00000505593.5:n.457+126dup (LOX)
ENST00000513319.5:n.474+126dup (LOX)
NM_001178102.1:c.441+126dup (LOX) NP_001171573.1:n.441+126dup
NM_001178102.2:c.441+126dup (LOX) NP_001171573.1:n.441+126dup
NM_001317073.1:c.240+126dup (LOX) NP_001304002.1:n.240+126dup
NM_002317.5:c.1131+126dup (LOX) NP_002308.2:n.1131+126dup
NM_002317.6:c.1131+126dup (LOX) NP_002308.2:n.1131+126dup
XM_017009111.2:c.1106-4946dup (SRFBP1) XP_016864600.2:n.1106-4946dup
NM_002317.7:c.1131+126dup (LOX) MANE Select NP_002308.2:n.1131+126dup