Canonical Allele Identifier: CA1578376284

Gene: LOX SRFBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122070098C= , CM000667.2:g.122070098C=	GRCh38
NC_000005.9:g.121405793C= , CM000667.1:g.121405793C=	GRCh37
NC_000005.8:g.121433692C=	NCBI36
NG_008722.1:g.13263G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.1202G= (LOX) MANE Select	ENSP00000231004.4:p.Arg401=
ENST00000639739.2:c.*394G= (LOX)	ENSP00000492324.2:n.*394G=
ENST00000231004.4:c.1202G= (LOX)	ENSP00000231004.4:p.Arg401=
ENST00000503759.5:n.793G= (LOX)
ENST00000504881.1:n.312-5217C= (SRFBP1)
ENST00000505593.5:n.528G= (LOX)
ENST00000513319.5:n.545G= (LOX)
NM_001178102.1:c.512G= (LOX)	NP_001171573.1:p.Arg171=
NM_001178102.2:c.512G= (LOX)	NP_001171573.1:p.Arg171=
NM_001317073.1:c.311G= (LOX)	NP_001304002.1:p.Arg104=
NM_002317.5:c.1202G= (LOX)	NP_002308.2:p.Arg401=
NM_002317.6:c.1202G= (LOX)	NP_002308.2:p.Arg401=
XM_017009111.2:c.1106-5217C= (SRFBP1)	XP_016864600.2:n.1106-5217C=
NM_002317.7:c.1202G= (LOX) MANE Select	NP_002308.2:p.Arg401=