Canonical Allele Identifier: CA446049971

Gene: LOX SRFBP1

Linked Data

• MyVariant Identifiers: chr5:g.121405828A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122070133A>T , CM000667.2:g.122070133A>T	GRCh38
NC_000005.9:g.121405828A>T , CM000667.1:g.121405828A>T	GRCh37
NC_000005.8:g.121433727A>T	NCBI36
NG_008722.1:g.13228T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.1167T>A (LOX) MANE Select	ENSP00000231004.4:p.Ser389=
ENST00000639739.2:c.*359T>A (LOX)	ENSP00000492324.2:n.*359T>A
ENST00000231004.4:c.1167T>A (LOX)	ENSP00000231004.4:p.Ser389=
ENST00000503759.5:n.758T>A (LOX)
ENST00000504881.1:n.312-5182A>T (SRFBP1)
ENST00000505593.5:n.493T>A (LOX)
ENST00000513319.5:n.510T>A (LOX)
NM_001178102.1:c.477T>A (LOX)	NP_001171573.1:p.Ser159=
NM_001178102.2:c.477T>A (LOX)	NP_001171573.1:p.Ser159=
NM_001317073.1:c.276T>A (LOX)	NP_001304002.1:p.Ser92=
NM_002317.5:c.1167T>A (LOX)	NP_002308.2:p.Ser389=
NM_002317.6:c.1167T>A (LOX)	NP_002308.2:p.Ser389=
XM_017009111.2:c.1106-5182A>T (SRFBP1)	XP_016864600.2:n.1106-5182A>T
NM_002317.7:c.1167T>A (LOX) MANE Select	NP_002308.2:p.Ser389=