Canonical Allele Identifier: CA360880197

Gene: LOX SRFBP1

Linked Data

• MyVariant Identifiers: chr5:g.121405787G>C (hg19) ; chr5:g.122070092G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122070092G>C , CM000667.2:g.122070092G>C	GRCh38
NC_000005.9:g.121405787G>C , CM000667.1:g.121405787G>C	GRCh37
NC_000005.8:g.121433686G>C	NCBI36
NG_008722.1:g.13269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.1208C>G (LOX) MANE Select	ENSP00000231004.4:p.Thr403Arg
ENST00000639739.2:c.*400C>G (LOX)	ENSP00000492324.2:n.*400C>G
ENST00000231004.4:c.1208C>G (LOX)	ENSP00000231004.4:p.Thr403Arg
ENST00000503759.5:n.799C>G (LOX)
ENST00000504881.1:n.312-5223G>C (SRFBP1)
ENST00000505593.5:n.534C>G (LOX)
ENST00000513319.5:n.551C>G (LOX)
NM_001178102.1:c.518C>G (LOX)	NP_001171573.1:p.Thr173Arg
NM_001178102.2:c.518C>G (LOX)	NP_001171573.1:p.Thr173Arg
NM_001317073.1:c.317C>G (LOX)	NP_001304002.1:p.Thr106Arg
NM_002317.5:c.1208C>G (LOX)	NP_002308.2:p.Thr403Arg
NM_002317.6:c.1208C>G (LOX)	NP_002308.2:p.Thr403Arg
XM_017009111.2:c.1106-5223G>C (SRFBP1)	XP_016864600.2:n.1106-5223G>C
NM_002317.7:c.1208C>G (LOX) MANE Select	NP_002308.2:p.Thr403Arg