Canonical Allele Identifier: CA360880310

Gene: LOX SRFBP1

Linked Data

• gnomAD v4: 5-122070143-A-C
• MyVariant Identifiers: chr5:g.121405838A>C (hg19) ; chr5:g.122070143A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122070143A>C , CM000667.2:g.122070143A>C	GRCh38
NC_000005.9:g.121405838A>C , CM000667.1:g.121405838A>C	GRCh37
NC_000005.8:g.121433737A>C	NCBI36
NG_008722.1:g.13218T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.1157T>G (LOX) MANE Select	ENSP00000231004.4:p.Val386Gly
ENST00000639739.2:c.*349T>G (LOX)	ENSP00000492324.2:n.*349T>G
ENST00000231004.4:c.1157T>G (LOX)	ENSP00000231004.4:p.Val386Gly
ENST00000503759.5:n.748T>G (LOX)
ENST00000504881.1:n.312-5172A>C (SRFBP1)
ENST00000505593.5:n.483T>G (LOX)
ENST00000513319.5:n.500T>G (LOX)
NM_001178102.1:c.467T>G (LOX)	NP_001171573.1:p.Val156Gly
NM_001178102.2:c.467T>G (LOX)	NP_001171573.1:p.Val156Gly
NM_001317073.1:c.266T>G (LOX)	NP_001304002.1:p.Val89Gly
NM_002317.5:c.1157T>G (LOX)	NP_002308.2:p.Val386Gly
NM_002317.6:c.1157T>G (LOX)	NP_002308.2:p.Val386Gly
XM_017009111.2:c.1106-5172A>C (SRFBP1)	XP_016864600.2:n.1106-5172A>C
NM_002317.7:c.1157T>G (LOX) MANE Select	NP_002308.2:p.Val386Gly