Canonical Allele Identifier: CA1578376369

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070319T= , CM000667.2:g.122070319T= GRCh38
NC_000005.9:g.121406014T= , CM000667.1:g.121406014T= GRCh37
NC_000005.8:g.121433913T= NCBI36
NG_008722.1:g.13042A=

Transcript Alleles

HGVS Amino-acid change
ENST00000231004.5:c.1132-151A= (LOX) MANE Select ENSP00000231004.4:n.1132-151A=
ENST00000639739.2:c.*324-151A= (LOX) ENSP00000492324.2:n.*324-151A=
ENST00000231004.4:c.1132-151A= (LOX) ENSP00000231004.4:n.1132-151A=
ENST00000503759.5:n.723-151A= (LOX)
ENST00000504881.1:n.312-4996T= (SRFBP1)
ENST00000505593.5:n.458-151A= (LOX)
ENST00000513319.5:n.475-151A= (LOX)
NM_001178102.1:c.442-151A= (LOX) NP_001171573.1:n.442-151A=
NM_001178102.2:c.442-151A= (LOX) NP_001171573.1:n.442-151A=
NM_001317073.1:c.241-151A= (LOX) NP_001304002.1:n.241-151A=
NM_002317.5:c.1132-151A= (LOX) NP_002308.2:n.1132-151A=
NM_002317.6:c.1132-151A= (LOX) NP_002308.2:n.1132-151A=
XM_017009111.2:c.1106-4996T= (SRFBP1) XP_016864600.2:n.1106-4996T=
NM_002317.7:c.1132-151A= (LOX) MANE Select NP_002308.2:n.1132-151A=