Canonical Allele Identifier: CA1578376363

Linked Data

dbSNP Id: rs1754412798

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070309del , CM000667.2:g.122070309del GRCh38
NC_000005.9:g.121406004del , CM000667.1:g.121406004del GRCh37
NC_000005.8:g.121433903del NCBI36
NG_008722.1:g.13054del

Transcript Alleles

HGVS Amino-acid change
ENST00000231004.5:c.1132-139del (LOX) MANE Select ENSP00000231004.4:n.1132-139del
ENST00000639739.2:c.*324-139del (LOX) ENSP00000492324.2:n.*324-139del
ENST00000231004.4:c.1132-139del (LOX) ENSP00000231004.4:n.1132-139del
ENST00000503759.5:n.723-139del (LOX)
ENST00000504881.1:n.312-5006del (SRFBP1)
ENST00000505593.5:n.458-139del (LOX)
ENST00000513319.5:n.475-139del (LOX)
NM_001178102.1:c.442-139del (LOX) NP_001171573.1:n.442-139del
NM_001178102.2:c.442-139del (LOX) NP_001171573.1:n.442-139del
NM_001317073.1:c.241-139del (LOX) NP_001304002.1:n.241-139del
NM_002317.5:c.1132-139del (LOX) NP_002308.2:n.1132-139del
NM_002317.6:c.1132-139del (LOX) NP_002308.2:n.1132-139del
XM_017009111.2:c.1106-5006del (SRFBP1) XP_016864600.2:n.1106-5006del
NM_002317.7:c.1132-139del (LOX) MANE Select NP_002308.2:n.1132-139del