Canonical Allele Identifier: CA446049986

Gene: LOX SRFBP1

Linked Data

• MyVariant Identifiers: chr5:g.121405855T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122070160T>A , CM000667.2:g.122070160T>A	GRCh38
NC_000005.9:g.121405855T>A , CM000667.1:g.121405855T>A	GRCh37
NC_000005.8:g.121433754T>A	NCBI36
NG_008722.1:g.13201A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.1140A>T (LOX) MANE Select	ENSP00000231004.4:p.Val380=
ENST00000639739.2:c.*332A>T (LOX)	ENSP00000492324.2:n.*332A>T
ENST00000231004.4:c.1140A>T (LOX)	ENSP00000231004.4:p.Val380=
ENST00000503759.5:n.731A>T (LOX)
ENST00000504881.1:n.312-5155T>A (SRFBP1)
ENST00000505593.5:n.466A>T (LOX)
ENST00000513319.5:n.483A>T (LOX)
NM_001178102.1:c.450A>T (LOX)	NP_001171573.1:p.Val150=
NM_001178102.2:c.450A>T (LOX)	NP_001171573.1:p.Val150=
NM_001317073.1:c.249A>T (LOX)	NP_001304002.1:p.Val83=
NM_002317.5:c.1140A>T (LOX)	NP_002308.2:p.Val380=
NM_002317.6:c.1140A>T (LOX)	NP_002308.2:p.Val380=
XM_017009111.2:c.1106-5155T>A (SRFBP1)	XP_016864600.2:n.1106-5155T>A
NM_002317.7:c.1140A>T (LOX) MANE Select	NP_002308.2:p.Val380=