Canonical Allele Identifier: CA1578376380

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070343_122070344delinsAT , CM000667.2:g.122070343_122070344delinsAT GRCh38
NC_000005.9:g.121406038_121406039delinsAT , CM000667.1:g.121406038_121406039delinsAT GRCh37
NC_000005.8:g.121433937_121433938delinsAT NCBI36
NG_008722.1:g.13017_13018delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.1131+150_1131+151delinsAT (LOX) MANE Select ENSP00000231004.4:n.1131+150_1131+151delinsAT
ENST00000639739.2:c.*323+150_*323+151delinsAT (LOX) ENSP00000492324.2:n.*323+150_*323+151delinsAT
ENST00000231004.4:c.1131+150_1131+151delinsAT (LOX) ENSP00000231004.4:n.1131+150_1131+151delinsAT
ENST00000503759.5:n.722+150_722+151delinsAT (LOX)
ENST00000504881.1:n.312-4972_312-4971delinsAT (SRFBP1)
ENST00000505593.5:n.457+150_457+151delinsAT (LOX)
ENST00000513319.5:n.474+150_474+151delinsAT (LOX)
NM_001178102.1:c.441+150_441+151delinsAT (LOX) NP_001171573.1:n.441+150_441+151delinsAT
NM_001178102.2:c.441+150_441+151delinsAT (LOX) NP_001171573.1:n.441+150_441+151delinsAT
NM_001317073.1:c.240+150_240+151delinsAT (LOX) NP_001304002.1:n.240+150_240+151delinsAT
NM_002317.5:c.1131+150_1131+151delinsAT (LOX) NP_002308.2:n.1131+150_1131+151delinsAT
NM_002317.6:c.1131+150_1131+151delinsAT (LOX) NP_002308.2:n.1131+150_1131+151delinsAT
XM_017009111.2:c.1106-4972_1106-4971delinsAT (SRFBP1) XP_016864600.2:n.1106-4972_1106-4971delinsAT
NM_002317.7:c.1131+150_1131+151delinsAT (LOX) MANE Select NP_002308.2:n.1131+150_1131+151delinsAT