Canonical Allele Identifier: CA446049977

Gene: LOX SRFBP1

Linked Data

• MyVariant Identifiers: chr5:g.121405837A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122070142A>G , CM000667.2:g.122070142A>G	GRCh38
NC_000005.9:g.121405837A>G , CM000667.1:g.121405837A>G	GRCh37
NC_000005.8:g.121433736A>G	NCBI36
NG_008722.1:g.13219T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.1158T>C (LOX) MANE Select	ENSP00000231004.4:p.Val386=
ENST00000639739.2:c.*350T>C (LOX)	ENSP00000492324.2:n.*350T>C
ENST00000231004.4:c.1158T>C (LOX)	ENSP00000231004.4:p.Val386=
ENST00000503759.5:n.749T>C (LOX)
ENST00000504881.1:n.312-5173A>G (SRFBP1)
ENST00000505593.5:n.484T>C (LOX)
ENST00000513319.5:n.501T>C (LOX)
NM_001178102.1:c.468T>C (LOX)	NP_001171573.1:p.Val156=
NM_001178102.2:c.468T>C (LOX)	NP_001171573.1:p.Val156=
NM_001317073.1:c.267T>C (LOX)	NP_001304002.1:p.Val89=
NM_002317.5:c.1158T>C (LOX)	NP_002308.2:p.Val386=
NM_002317.6:c.1158T>C (LOX)	NP_002308.2:p.Val386=
XM_017009111.2:c.1106-5173A>G (SRFBP1)	XP_016864600.2:n.1106-5173A>G
NM_002317.7:c.1158T>C (LOX) MANE Select	NP_002308.2:p.Val386=