Canonical Allele Identifier: CA1578376358

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070299C= , CM000667.2:g.122070299C= GRCh38
NC_000005.9:g.121405994C= , CM000667.1:g.121405994C= GRCh37
NC_000005.8:g.121433893C= NCBI36
NG_008722.1:g.13062G=

Transcript Alleles

HGVS Amino-acid change
ENST00000231004.5:c.1132-131G= (LOX) MANE Select ENSP00000231004.4:n.1132-131G=
ENST00000639739.2:c.*324-131G= (LOX) ENSP00000492324.2:n.*324-131G=
ENST00000231004.4:c.1132-131G= (LOX) ENSP00000231004.4:n.1132-131G=
ENST00000503759.5:n.723-131G= (LOX)
ENST00000504881.1:n.312-5016C= (SRFBP1)
ENST00000505593.5:n.458-131G= (LOX)
ENST00000513319.5:n.475-131G= (LOX)
NM_001178102.1:c.442-131G= (LOX) NP_001171573.1:n.442-131G=
NM_001178102.2:c.442-131G= (LOX) NP_001171573.1:n.442-131G=
NM_001317073.1:c.241-131G= (LOX) NP_001304002.1:n.241-131G=
NM_002317.5:c.1132-131G= (LOX) NP_002308.2:n.1132-131G=
NM_002317.6:c.1132-131G= (LOX) NP_002308.2:n.1132-131G=
XM_017009111.2:c.1106-5016C= (SRFBP1) XP_016864600.2:n.1106-5016C=
NM_002317.7:c.1132-131G= (LOX) MANE Select NP_002308.2:n.1132-131G=