Canonical Allele Identifier: CA360880288

Gene: LOX SRFBP1

Linked Data

• MyVariant Identifiers: chr5:g.121405827C>A (hg19) ; chr5:g.122070132C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122070132C>A , CM000667.2:g.122070132C>A	GRCh38
NC_000005.9:g.121405827C>A , CM000667.1:g.121405827C>A	GRCh37
NC_000005.8:g.121433726C>A	NCBI36
NG_008722.1:g.13229G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.1168G>T (LOX) MANE Select	ENSP00000231004.4:p.Asp390Tyr
ENST00000639739.2:c.*360G>T (LOX)	ENSP00000492324.2:n.*360G>T
ENST00000231004.4:c.1168G>T (LOX)	ENSP00000231004.4:p.Asp390Tyr
ENST00000503759.5:n.759G>T (LOX)
ENST00000504881.1:n.312-5183C>A (SRFBP1)
ENST00000505593.5:n.494G>T (LOX)
ENST00000513319.5:n.511G>T (LOX)
NM_001178102.1:c.478G>T (LOX)	NP_001171573.1:p.Asp160Tyr
NM_001178102.2:c.478G>T (LOX)	NP_001171573.1:p.Asp160Tyr
NM_001317073.1:c.277G>T (LOX)	NP_001304002.1:p.Asp93Tyr
NM_002317.5:c.1168G>T (LOX)	NP_002308.2:p.Asp390Tyr
NM_002317.6:c.1168G>T (LOX)	NP_002308.2:p.Asp390Tyr
XM_017009111.2:c.1106-5183C>A (SRFBP1)	XP_016864600.2:n.1106-5183C>A
NM_002317.7:c.1168G>T (LOX) MANE Select	NP_002308.2:p.Asp390Tyr