Canonical Allele Identifier: CA1578379795
Gene: LOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122077668C= , CM000667.2:g.122077668C= GRCh38
NC_000005.9:g.121413363C= , CM000667.1:g.121413363C= GRCh37
NC_000005.8:g.121441262C= NCBI36
NG_008722.1:g.5693G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.318G= MANE Select ENSP00000231004.4:p.Thr106=
ENST00000639739.2:c.318G= ENSP00000492324.2:p.Thr106=
ENST00000231004.4:c.318G= ENSP00000231004.4:p.Thr106=
NM_002317.5:c.318G= NP_002308.2:p.Thr106=
NM_002317.6:c.318G= NP_002308.2:p.Thr106=
NM_002317.7:c.318G= MANE Select NP_002308.2:p.Thr106=